# FDA Inspection 677216 - Bredent GmbH & Co. KG - July 29, 2010

Source: https://www.keypedia.com/records/fda_inspections/bredent-gmbh-co-kg/caeab446-0859-4433-b179-3f656b116510
Source feed: FDA_Inspections

> FDA Inspection 677216 for Bredent GmbH & Co. KG on July 29, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 677216
- Company Name: Bredent GmbH & Co. KG
- Inspection Date: 2010-07-29
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 852293 - 2013-09-19](https://www.keypedia.com/records/fda_inspections/bredent-gmbh-co-kg/ed3df42e-b3b3-4463-9b3d-9ba85e6ffa0d)

Company: https://www.keypedia.com/companies/bredent-gmbh-co-kg/b357c2ee-3fd8-4868-b9c8-93702ae7fbdb

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