# Audifon Gmbh – FDA Inspection, May 11, 2017

Source: https://www.keypedia.com/records/fda_inspections/audifon-gmbh/6facc4a2-ac66-4f8d-8c73-43c79f536569
Source feed: FDA_Inspections

> FDA inspection 1013135 of Audifon Gmbh, May 11, 2017. Classification: Voluntary Action Indicated (VAI). 9 citations under 21 CFR parts 803 and 820. Form 483 issued. 2 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1013135
- Company Name: Audifon Gmbh
- Inspection Date: 2017-05-11
- 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: 9

## Related Documents

- [FDA Inspection 1260616 - 2025-01-16](https://www.keypedia.com/records/fda_inspections/audifon-gmbh/1b27d5b8-fd89-4a66-9d93-b33bac1ad25b)
- FDA Inspection 1114379 - 2019-12-18

## Related Officers

- [Joshua J. Silvestri](https://www.keypedia.com/people/joshua-j-silvestri/433e29b3-ce5f-44d2-9984-7a6cb61e1824)

Company: https://www.keypedia.com/companies/audifon-gmbh/f0e62de7-b5b5-49b3-b8ec-b08e46b3f773

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