# CeramTec GmbH, Medical Products Division – FDA Inspection, Feb 9, 2012

Source: https://www.keypedia.com/records/fda_inspections/ceramtec-gmbh-medical-products-division/fc13c4b9-7471-4e1e-a589-f0624617a7d5
Source feed: FDA_Inspections

> FDA inspection 773131 of CeramTec GmbH, Medical Products Division, February 09, 2012. Classification: No Action Indicated (NAI). 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 773131
- Company Name: CeramTec GmbH, Medical Products Division
- Inspection Date: 2012-02-09
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1198717 - 2023-02-09
- [FDA Inspection 1041074 - 2018-02-14](https://www.keypedia.com/records/fda_inspections/ceramtec-gmbh-medical-products-division/efa786bf-a0cc-4a94-9524-939d7da0f593)
- FDA Inspection 932190 - 2015-06-10

Company: https://www.keypedia.com/companies/ceramtec-gmbh-medical-products-division/e37d74ea-0e1d-4ae0-bf77-e401fe3e7eda

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