# Audifon Gmbh – FDA Inspection, Jan 16, 2025

Source: https://www.keypedia.com/records/fda_inspections/audifon-gmbh/1b27d5b8-fd89-4a66-9d93-b33bac1ad25b
Source feed: FDA_Inspections

> FDA inspection 1260616 of Audifon Gmbh, January 16, 2025. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1260616
- Company Name: Audifon Gmbh
- Inspection Date: 2025-01-16
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Office of Inspections and Investigations
- Citation Count: 6

## Related Documents

- FDA Inspection 1114379 - 2019-12-18
- [FDA Inspection 1013135 - 2017-05-11](https://www.keypedia.com/records/fda_inspections/audifon-gmbh/6facc4a2-ac66-4f8d-8c73-43c79f536569)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/sunita-pandey/008e5bb8-0eb3-45d8-8524-734ac0454250)

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

Office: https://www.keypedia.com/offices/office-of-inspections-and-investigations/7dd0b904-a3df-46bc-a7b2-70ddb6f809c8