# CeramTec GmbH, Medical Products Division, Marktredwitz, Germany – FDA Inspections

Source: https://www.keypedia.com/companies/ceramtec-gmbh-medical-products-division/aeab5264-3819-4f6c-8993-8ad5023fdf33

> Inspection records and compliance data for CeramTec GmbH, Medical Products Division in Marktredwitz. 4 FDA inspections on record, 2 Form 483s, last inspected January 19, 2023.

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## Details

- Name: CeramTec GmbH, Medical Products Division
- FEI Number: 3001278222
- Address Line 1: Ceramtec-Weg 1
- City: Marktredwitz
- Country Name: Germany
- Address: Ceramtec-Weg 1, Marktredwitz, Germany
- Country: Germany

## Related Documents

- [FDA Inspection 1197933 - CeramTec GmbH, Medical Products Division - 2023-01-19](https://www.keypedia.com/records/fda_inspections/ceramtec-gmbh-medical-products-division/2060b8f3-8c8c-4a5b-af24-0e4e115dfe33) — source: FDA, date: January 19, 2023
- FDA Inspection 1041252 - CeramTec GmbH, Medical Products Division - 2018-02-16 — classification: No Action Indicated (NAI), source: FDA, date: February 16, 2018
- [FDA Inspection 1041252 - CeramTec GmbH, Medical Products Division - 2018-02-16](https://www.keypedia.com/records/fda_inspections/ceramtec-gmbh-medical-products-division/d0d6fb89-4ccc-4b48-931a-04a756d6607e) — classification: No Action Indicated (NAI), source: FDA, date: February 16, 2018
- FDA Inspection 932193 - CeramTec GmbH, Medical Products Division - 2015-06-12 — classification: No Action Indicated (NAI), source: FDA, date: June 12, 2015
- FDA Inspection 665629 - CeramTec GmbH, Medical Products Division - 2010-04-29 — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 29, 2010
- [FDA Inspection 665629 - CeramTec GmbH, Medical Products Division - 2010-04-29](https://www.keypedia.com/records/fda_inspections/ceramtec-gmbh-medical-products-division/34779fc4-18a8-483a-8dd2-508c9020ae22) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 29, 2010

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