# Audifon-USA, Inc. – FDA Inspection, Apr 1, 2010

Source: https://www.keypedia.com/records/fda_inspections/audifon-usa-inc/9f8b2688-bbc5-4076-96ca-5db950e7fd74
Source feed: FDA_Inspections

> FDA inspection 654100 of Audifon-USA, Inc., April 01, 2010. Classification: Voluntary Action Indicated (VAI). 8 citations under 21 CFR part 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 654100
- Company Name: Audifon-USA, Inc.
- Inspection Date: 2010-04-01
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 8

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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