# FDA Inspection 831106 - Audifon-USA, Inc. - May 08, 2013

Source: https://www.globalkeysolutions.net/records/fda_inspections/audifon-usa-inc/937a0ac7-918b-4f36-bc74-849f1b65422e
Source feed: FDA_Inspections

> FDA Inspection 831106 for Audifon-USA, Inc. on May 08, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 831106
- Company Name: Audifon-USA, Inc.
- Inspection Date: 2013-05-08
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 831106 - 2013-05-08](https://www.globalkeysolutions.net/records/fda_inspections/audifon-usa-inc/21917cd6-5044-4d9c-8d40-bb983c82f7f5)

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

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