# Audifon-USA, Inc. – FDA Inspection, Nov 27, 2018

Source: https://www.keypedia.com/records/fda_inspections/audifon-usa-inc/ee0749f2-572d-484c-8683-89566b3f00c8
Source feed: FDA_Inspections

> FDA inspection 1072952 of Audifon-USA, Inc., November 27, 2018. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1072952
- Company Name: Audifon-USA, Inc.
- Inspection Date: 2018-11-27
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- [FDA Inspection 978529 - 2016-07-14](https://www.keypedia.com/records/fda_inspections/audifon-usa-inc/b8df1358-f8a4-4cb8-a70b-37296ba827c7)
- [FDA Inspection 831106 - 2013-05-08](https://www.keypedia.com/records/fda_inspections/audifon-usa-inc/937a0ac7-918b-4f36-bc74-849f1b65422e)
- [FDA Inspection 654100 - 2010-04-01](https://www.keypedia.com/records/fda_inspections/audifon-usa-inc/9f8b2688-bbc5-4076-96ca-5db950e7fd74)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/richard-k-vogel/3ddd8bff-24fd-40ee-b0a7-fb5333a520f5)

Company: https://www.keypedia.com/companies/audifon-usa-inc/c7c3a3e6-4877-40b6-bae9-8a4ba26af98a

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7