# FDA Inspection 719704 - Heraeus Kulzer GmbH - March 10, 2011

Source: https://www.globalkeysolutions.net/records/fda_inspections/heraeus-kulzer-gmbh/fb261a0e-bf95-47ab-ab61-992cd15548f5/
Source feed: FDA_Inspections

> FDA Inspection 719704 for Heraeus Kulzer GmbH on March 10, 2011. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 719704
- Company Name: Heraeus Kulzer GmbH
- Inspection Date: 2011-03-10
- Classification: Official Action Indicated (OAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 719704 - 2011-03-10](https://www.globalkeysolutions.net/api/records/fda_inspections/heraeus-kulzer-gmbh/97625a7e-af4c-4882-9520-4b93f8969628/)

Company: https://www.globalkeysolutions.net/companies/heraeus-kulzer-gmbh/1157fdb6-a23f-4bc1-9212-f2dd099ff0cf

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