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

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

> Inspection records and compliance data for CeramTec GmbH, Medical Products Division in Plochingen. 4 FDA inspections on record, 1 Form 483, last inspected February 09, 2023.

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## Details

- Name: CeramTec GmbH, Medical Products Division
- FEI Number: 3002806653
- Address Line 1: Building K, Ceramtec-Platz 1-9
- City: Plochingen
- Country Name: Germany
- Address: Building K, Ceramtec-Platz 1-9, Plochingen, Germany
- Country: Germany

## Related Documents

- FDA Inspection 1198717 - CeramTec GmbH, Medical Products Division - 2023-02-09 — classification: No Action Indicated (NAI), source: FDA, date: February 9, 2023
- FDA Inspection 1041074 - CeramTec GmbH, Medical Products Division - 2018-02-14 — classification: No Action Indicated (NAI), source: FDA, date: February 14, 2018
- [FDA Inspection 1041074 - CeramTec GmbH, Medical Products Division - 2018-02-14](https://www.keypedia.com/records/fda_inspections/ceramtec-gmbh-medical-products-division/efa786bf-a0cc-4a94-9524-939d7da0f593) — classification: No Action Indicated (NAI), source: FDA, date: February 14, 2018
- FDA Inspection 1041074 - CeramTec GmbH, Medical Products Division - 2018-02-14 — classification: No Action Indicated (NAI), source: FDA, date: February 14, 2018
- FDA Inspection 932190 - CeramTec GmbH, Medical Products Division - 2015-06-10 — classification: No Action Indicated (NAI), source: FDA, date: June 10, 2015
- FDA Inspection 932190 - CeramTec GmbH, Medical Products Division - 2015-06-10 — classification: No Action Indicated (NAI), source: FDA, date: June 10, 2015
- FDA Inspection 773131 - CeramTec GmbH, Medical Products Division - 2012-02-09 — classification: No Action Indicated (NAI), source: FDA, date: February 9, 2012
- [FDA Inspection 773131 - CeramTec GmbH, Medical Products Division - 2012-02-09](https://www.keypedia.com/records/fda_inspections/ceramtec-gmbh-medical-products-division/fc13c4b9-7471-4e1e-a589-f0624617a7d5) — classification: No Action Indicated (NAI), source: FDA, date: February 9, 2012

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