# FDA Inspection 1013135 - Audifon Gmbh - 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 for Audifon Gmbh on May 11, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1013135
- Company Name: Audifon Gmbh
- Inspection Date: 2017-05-11
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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