# FDA Inspection 665629 - CeramTec GmbH, Medical Products Division - April 29, 2010

Source: https://www.globalkeysolutions.net/records/fda_inspections/ceramtec-gmbh-medical-products-division/34779fc4-18a8-483a-8dd2-508c9020ae22
Source feed: FDA_Inspections

> FDA Inspection 665629 for CeramTec GmbH, Medical Products Division on April 29, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 665629
- Company Name: CeramTec GmbH, Medical Products Division
- Inspection Date: 2010-04-29
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 665629 - 2010-04-29](https://www.globalkeysolutions.net/records/fda_inspections/ceramtec-gmbh-medical-products-division/0b2ef9fb-f859-447c-ae70-64f964732e13)

Company: https://www.globalkeysolutions.net/companies/ceramtec-gmbh-medical-products-division/aeab5264-3819-4f6c-8993-8ad5023fdf33

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