# FDA Inspection 931622 - Vitaphone GmbH - May 08, 2015

Source: https://www.keypedia.com/records/fda_inspections/vitaphone-gmbh/cc603d47-9415-447a-ac30-01f465d19959
Source feed: FDA_Inspections

> FDA Inspection 931622 for Vitaphone GmbH on May 08, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 931622
- Company Name: Vitaphone GmbH
- Inspection Date: 2015-05-08
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 931622 - 2015-05-08](https://www.keypedia.com/records/fda_inspections/vitaphone-gmbh/710e7ae5-9c42-4617-a9ce-0a8cd9ed6303)

Company: https://www.keypedia.com/companies/vitaphone-gmbh/b5feab83-b1b5-4194-a3e9-397da7e14cc6

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