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Daily Maintenance and Calibration Requirements for Audiometers Used in Occupational Hearing Testing

Daily Maintenance and Calibration Requirements for Audiometers Used in Occupational Hearing Testing
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There have never been better audiometer options for occupational hearing testing than what’s available now. Despite the advances in technology, there are still quick verification tasks that will help ensure that your testing equipment is performing the way it should every day of testing. Modern audiometers and headsets often offer interesting features to allow for daily verification tasks, routine maintenance, and associated record-keeping. In this chapter, we will be reviewing each of those tasks to help illustrate what maintenance you need to perform to help you meet OSHA hearing testing compliance.

Annual Calibration

All hearing testing systems should be calibrated at least once every 12 months. Historically, audiometers often remained stationary and were calibrated by a technician who visited the site where the OSHA-compliant audiometer was being used and provided a calibration report and associated correction factors. With advancements in technology, both in audiometer capabilities and the improvement in robustness in hardware components in audiometric headsets, calibration can look a little different than in years past. For computerized and tablet-based audiometers, a full calibration can be obtained by testing the headset alone and providing calibration correction factors. These calculations are then applied to the software resulting in a re-calibrated system.

ANSI/ASA S3.6 specifies that all clinical audiometers need to be calibrated at a minimum every 12 months. OSHA 29 CFR 1910.95 differentiates between periodic and exhaustive calibrations; however, once a system or headset is on-hand for calibration, most calibrators will opt for an exhaustive calibration, which in turn meets the ANSI specifications as well as the ones specified by OSHA.

Daily Functional Check

The purpose of the Daily Functional Check is to ensure that the cable connections are interruption-free and that there is no abnormality (static, volume changes) in the sound output of the testing system. For this test, ANSI recommends using a 1000 Hz tone at 70 dB(HL) and requests that the test administrator put on the headphones and present these tones one at a time in each ear, all while putting slight pressure on the headphone jack connectors, and wiggling the cables to listen for any abnormalities. The tone presentation time should be approximately 20 seconds on each ear to allow for adequate manipulation of the jacks and cables. Should abnormalities be discovered, these should be addressed prior to continuing with testing. The Daily Functional Check is a static one-time verification each testing day, and the results should be recorded to help with the possible future investigation of an emerging equipment issue or in the case of an audit request for
equipment verification practices.

Daily Biological Verification

The Biological Verification aims to ensure that there hasn’t been significant sound output drift on a per-frequency basis since the last annual calibration. In order to set up this test, it is recommended that you create a distinct result file for this purpose for each individual who may administer workplace hearing testing. For example, creating a file with the patient name ‘Biological Verification A.A.’ under which every test can be saved and compared to baseline. Only individuals with stable hearing levels should perform Biological Verification.

After the first test for an individual has been marked as a ‘baseline,’ each test after that can be compared frequency-by-frequency for deviations of more than 10 dB(HL). Should there be deviations of more than 10 dB(HL), the system will require additional attention, and we would recommend contacting your Professional Supervisor or Hearing Conservation Program Administrator for recommended next steps.

Example of a Biological Verification Comparison:

Biological Verification: A.A. (tester’s Initials)
Test date ear Test Frequency (Hz) Threshold Result in dB(HL)
500 1000 2000 3000 4000 6000 8000
July 30, 2019 L 5 0 0 5 10 15 15
R 0 5 0 0 5 10 15
April 17, 2020 L 5 5 0 5 5 10 15
R 5 5 10 5 20* 30* 30*
Regular Test Day R 5 5 10 5 20* 30* 30*

* frequencies outside of the accepted range of variation of 10 dB(HL)

Everyday Troubleshooting

You may want to add additional verification measures if you notice wear and tear on the device or headphones. For example, a tear or fraying with any portion of the headphones. It’s possible for the headband or adjustment stems of the headphones to become warped or loose. If the headband is loose, you can apply gentle pressure on both sides to reshape the curvature of the band. Should corrosion or deposits be noted on the headphone jack (it could be green, black, or clear in colour), cleaning the jack with an alcohol wipe and allowing it to dry before plugging it back in is recommended.
It goes without saying that if a system is dropped, exposed to extreme temperature fluctuations, or compromised in any other significant fashion, all components should be reverified in the manners described above. In abiding by these practices, you can be fully confident that your audiometric system is providing accurate hearing testing results throughout the whole year through.
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Frequently Asked Questions

What are OSHA's three levels of audiometer calibration and how do they differ?

OSHA’s audiometer calibration framework operates at three levels. Daily functional check (29 CFR 1910.95(h)(5)(i)): performed before each testing day using a person with known stable hearing thresholds to confirm clean tone output without distortion or interruption. If any frequency shows a 10 dB or greater deviation from the listener’s known threshold, acoustic calibration is required before testing continues. Annual acoustic calibration (29 CFR 1910.95(h)(5)(ii)): a calibrated measurement of the audiometer’s output using laboratory instruments per Appendix E. If any frequency deviates 15 dB or more from ANSI standards, an exhaustive calibration is required. Exhaustive calibration (29 CFR 1910.95(h)(5)(iii)): a comprehensive recalibration of all audiometer parameters per ANSI S3.6, required at minimum every 2 years. This is the most rigorous level and typically requires specialized equipment. SHOEBOX: SHOEBOX’s annual calibration service performs acoustic calibration at every service interval. The advance-replacement model means no testing downtime between calibration cycles — the replacement transducer arrives calibrated and ready before the existing one is returned.

What qualifies as a biological verification, and who should perform it?

Biological verification is the daily functional check required by OSHA before each day of testing. The purpose is to detect significant drift in the audiometer’s sound output since the last annual calibration — not to evaluate the examiner’s hearing health. The check involves running a full audiogram on an individual with known stable hearing thresholds and comparing those results against that individual’s personal baseline. A deviation of 10 dB or more at any frequency indicates that the audiometer’s output has drifted and requires acoustic calibration. Any person with stable hearing thresholds can perform this function — the examiner does not need to have audiometrically normal hearing, only hearing that is stable and consistently documented. Individuals with hearing loss qualify if their thresholds are stable and their baseline is accurately recorded in the system. SHOEBOX: SHOEBOX PureTest’s daily calibration workflow guides the examiner through the biological verification step before testing begins, and logs the result as part of the session’s compliance documentation.

What criteria should an EHS Director use when evaluating audiometric testing technology?

Five categories matter. Compliance integrity: does the system meet ANSI S3.6, OSHA 1910.95, and MSHA requirements? Is it an FDA-listed medical device? Does it perform all required frequencies per ear? Does STS detection follow OSHA methodology precisely? Does it support boothless testing with documented ambient noise monitoring? Workflow integration: does the system fit how testing actually occurs at your facilities — shift patterns, location access, employee throughput needs? Data management: where do records go? Who controls access? Can historical audiograms be imported? Can results be exported for regulatory reporting? Professional oversight: does the system support the Professional Supervisor and Audiology Reviewer workflow, or require managing that separately? Total program cost: equipment, calibration, professional services, data management, and technician time — compared against what you currently pay per test. SHOEBOX: SHOEBOX PureTest addresses all five evaluation categories — ANSI S3.6 and FDA-listed compliance, on-site workflow integration, cloud-based data management with import and export, built-in Professional Supervisor and Audiology Reviewer support through SHOEBOX Audiological Services, and a predictable per-unit subscription cost model.

How long must audiometric records be retained, and what happens to them when an employee leaves?

OSHA requires that all employee audiometric test records be retained for the duration of that employee’s employment (29 CFR 1910.95(m)(3)(ii)). This requirement applies regardless of whether the employee leaves voluntarily, is terminated, or retires. Noise exposure measurement records carry a shorter retention period: 2 years from the date of measurement (29 CFR 1910.95(m)(3)(i)). Three operational implications follow. First, records must be accessible — not just stored. OSHA requires that audiometric records be made available to employees, former employees, designated representatives, and OSHA upon request (29 CFR 1910.95(m)(4)). Records that cannot be produced promptly on request do not meet this requirement regardless of where they are stored. Second, if a business closes or is acquired, audiometric records must be transferred to the successor employer, or if there is none, employees and NIOSH must be notified before disposal (29 CFR 1910.95(m)(5)). Third, the audiometric record is not just a test result — it must include the employee’s name and job classification, the test date, the examiner’s name, the date of the most recent acoustic calibration, the employee’s most recent noise exposure assessment, and the background sound pressure levels in the test room at the time of testing (29 CFR 1910.95(m)(2)(ii)). SHOEBOX: The SHOEBOX Data Management Portal stores the complete required record set — audiogram results, examiner identity, calibration dates, and ambient noise measurements — with automatic backup from the iPad. Records are accessible on demand without submitting a request to an external vendor, and they remain in the portal regardless of changes to the organization’s equipment or service provider.

What triggers the need for an audiogram to be sent to an Audiology Reviewer?

Two conditions generate mandatory review under OSHA. First, any audiogram in which a standard threshold shift has been identified must be reviewed by an audiologist, otolaryngologist, or physician, who determines whether the shift requires further evaluation (29 CFR 1910.95(g)(7)(iii)). Second, “problem audiograms” — those that suggest pathology, testing validity concerns, or clinical findings beyond what STS criteria capture — require professional evaluation. Problem audiograms may show: sudden drops at a single frequency, significant asymmetry between ears, audiometric configurations inconsistent with noise exposure patterns, or results that suggest the test was not completed under valid conditions. OSHA does not define “problem audiogram” with a numerical standard; the determination is a clinical judgment that requires a professional reviewer, not a software rule. SHOEBOX: SHOEBOX’s automatic triage system routes audiograms that meet configured criteria (STS detected, problem audiogram flags, incomplete results) directly to the Audiology Review Network queue in the portal — without requiring the EHS Manager to manually identify and forward files.

What does an Audiology Reviewer consider when deciding whether to revise a baseline audiogram?

Baseline revision is indicated under two circumstances per OSHA: when an STS is deemed persistent (29 CFR 1910.95(g)(9)(i)) and when the annual audiogram shows significant improvement over the established baseline (29 CFR 1910.95(g)(9)(ii)). In practice, reviewers also consider: whether the current audiogram represents the employee’s true hearing status versus a transient shift; whether prior baseline errors (such as a baseline recorded during a TTS) should be corrected; and whether the pattern of results across multiple years is consistent. The decision to revise a baseline audiogram must be made by a qualified professional — it is a clinical determination, not an automatic rule. An incorrect baseline revision can suppress future STS detection for years.

What are the most common drivers for transitioning from a mobile van service to in-house testing?

Four operational patterns consistently drive the decision. Scheduling compression: concentrating all program testing into one or two van days per year creates a high-stakes logistics exercise where a portion of employees typically miss their appointment, each requiring individual rescheduling. Delayed access to results: results arrive weeks after the van visit in a batch report, which compresses timelines for STS notification, retest scheduling, and follow-up actions. Baseline timeline gaps: new hires cannot be baselined until the next van visit, often months after first noise exposure, triggering the HPD-wearing requirement during that gap. Per-test cost: mobile testing fees increase predictably with headcount and typically include travel, technician time, and data management charges that compound at scale. When organizations evaluate these costs alongside the operational control and direct data access that in-house testing provides, the transition often shows a clear financial and compliance case. SHOEBOX: When organizations bring testing in-house with SHOEBOX, commonly reported outcomes include reduced per-test costs, improved retest completion rates, new-hire baselines obtained within days of hire, and consistent protocol enforcement across all test examiners.

How should we handle audiometric records from our previous service provider when transitioning to SHOEBOX?

Historical record quality varies significantly by source. Paper audiograms from clinic visits, CSV exports from legacy audiometric software, and data from previous service provider platforms all require different handling. The first priority is establishing accurate baselines in the new system: many transition complications arise from importing incorrect or outdated baselines, which causes STS determinations to be made against the wrong reference point. SHOEBOX Customer Success provides data import services to facilitate migration, including baseline verification and mapping from common legacy formats. Before importing, it is worth reviewing whether the historical baselines on file are actually the best baselines for each employee — in some cases, a fresh baseline under controlled conditions is preferable to importing a suspect historical record.

What are the compliance and operational advantages of iPad-based audiometry for service providers managing multi-client programs?

Service providers running audiometric testing across multiple employer clients face a consistency problem that traditional equipment creates: different sites, different technicians, different ambient conditions, and different testing schedules produce protocol variation that affects data quality. iPad-based audiometry addresses this structurally. Pre-configured test settings — locked by the administrator — ensure the same protocol is applied across every client, every site, every technician. The REACT™ Safeguards system monitors ambient noise and response validity throughout each session, flagging conditions that could compromise results rather than leaving those assessments to individual examiner judgment. Centralized data management across all client programs provides a single point of access for scheduling, reporting, and billing — without managing data in multiple formats from multiple sites. SHOEBOX: SHOEBOX PureTest provides this consistency layer for service providers. Administrator-locked test configurations, REACT Safeguards, and the centralized Data Management Portal are the specific features that address protocol variation across multi-client programs.

What are the technician qualification requirements for service providers administering audiometric tests?

Under 29 CFR 1910.95(g)(3), technicians performing audiometric tests must be responsible to an audiologist, otolaryngologist, or physician — and must either hold CAOHC certification, have satisfactorily demonstrated competence, or be operating a microprocessor audiometer (for which the certification requirement does not apply). For service providers, the practical implication is that CAOHC certification remains the recognized industry credential, and clients often require it as an assurance of technician competence. The microprocessor exception allows service providers to deploy non-CAOHC technicians with SHOEBOX, but program-level Professional Supervisor oversight is still required regardless. Service providers should document the supervisory relationship clearly in their client program agreements.

What is the complete step-by-step workflow for an OSHA-compliant testing day?

A compliant testing day follows nine sequential steps. Step 1 — Daily calibration: headphones check, room scan, and biological verification must be completed before any employee testing begins; OSHA requires the functional check before each day’s use (29 CFR 1910.95(h)(5)(i)). Step 2 — Room scan confirmation: the room scan result must be documented before testing starts; if the room fails, testing cannot proceed in that location. Step 3 — Employee intake: confirm employee identity, retrieve demographic data, verify noise exposure assessment and baseline status. Step 4 — Pre-test instruction: orient the employee to the test interface and response method; ensure they understand the task before tones begin. Step 5 — Testing: run automated, assisted, or manual mode as appropriate; REACT™ Safeguards monitor ambient noise and response patterns throughout. Step 6 — Digital signature: both employee and examiner sign the audiogram record on-device. Step 7 — Result review: STS is calculated automatically; examiner confirms test is complete and valid. Step 8 — Triage: audiogram is reviewed against configured rules; STS or problem audiogram flags route the file to the appropriate next action. Step 9 — Sync: completed audiograms upload to the portal when connectivity is available. SHOEBOX: This nine-step workflow maps directly to the SHOEBOX PureTest testing flow. Steps 1–2 correspond to PureTest’s daily calibration and room scan sequence; Steps 3–7 run within the PureTest app on the iPad; Steps 8–9 are handled by the Data Management Portal’s triage and sync functions.

Why is the baseline audiogram the most important record in an employee's Hearing Conservation Program file?

The baseline audiogram is the reference against which every future STS determination is made. Every annual audiogram compares the employee’s current thresholds to their baseline at 2,000, 3,000, and 4,000 Hz. An inaccurate baseline — established while the employee had a temporary threshold shift from recent noise exposure, illness, or the wrong 14-hour quiet period — compresses or inflates the apparent shift in every subsequent comparison. A baseline established too high (during a TTS) understates future STS risk. A baseline established too low may trigger false STSs. OSHA requires a minimum 14-hour quiet period before baseline testing (29 CFR 1910.95(g)(5)(iii)); hearing protectors may substitute for this requirement. The clinical integrity of the entire Hearing Conservation Program rests on the accuracy of the baseline. SHOEBOX: SHOEBOX Data Management PLUS manages baseline assignment and revision per employee. The portal’s triage system automatically flags cases where a persistent STS may warrant baseline revision and routes them to an Audiology Reviewer for clinical determination.

When should a baseline audiogram be revised, and who makes that decision?

Baseline revision is indicated in two circumstances under OSHA (29 CFR 1910.95(g)(9)): when a threshold shift is determined to be persistent (it has not resolved after retest), and when a subsequent audiogram shows significant improvement over the established baseline. The decision to revise a baseline audiogram must be made by a qualified professional — an audiologist, otolaryngologist, or physician. It is not a software function. The operational implication: programs that lack access to a professional reviewer may be unable to revise baselines appropriately, which causes either persistent false STSs (if improvement goes unrecognized) or missed STSs (if a persistent shift becomes the new assumed baseline without formal revision).

How does the testing environment affect employee participation rates?

Employee participation in annual audiometric testing is affected by how the experience is structured. Traditional mobile van testing — employees waiting in line, testing in a small shared space, uncertain timing during shift changes — creates friction that contributes to no-shows and reluctant participation. Testing at the employee’s own workplace, on their schedule, in a familiar environment, removes most of that friction. The testing interface also matters: an interface that communicates clearly in the employee’s language, responds predictably, and takes a reasonable amount of time increases completion rates. Long tests, confusing instructions, or uncomfortable equipment reduce them. SHOEBOX: SHOEBOX PureTest’s interface — where the employee drags an on-screen disc to indicate heard or not-heard — is largely language-agnostic, making it accessible for multilingual workforces. The system supports English, French, and Spanish for examiner-facing content. Automated mode tests are typically completed in a few minutes per ear.

Two ways to start. Both take 15 minutes.

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