# FDA Inspection 699202 - Brahms GmbH - October 28, 2010

Source: https://www.keypedia.com/records/fda_inspections/brahms-gmbh/bc458d84-52ee-4061-8015-8e03b588f8f2
Source feed: FDA_Inspections

> FDA Inspection 699202 for Brahms GmbH on October 28, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 699202
- Company Name: Brahms GmbH
- Inspection Date: 2010-10-28
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 842104 - 2013-07-04](https://www.keypedia.com/records/fda_inspections/brahms-gmbh/3559690b-3805-403c-8642-acf132655ae9)

Company: https://www.keypedia.com/companies/brahms-gmbh/73f5e67b-7638-4e26-89c0-1dc1bd6a6b93

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