# CeramTec GmbH, Medical Products Division – FDA Inspection, Feb 16, 2018

Source: https://www.keypedia.com/records/fda_inspections/ceramtec-gmbh-medical-products-division/d0d6fb89-4ccc-4b48-931a-04a756d6607e
Source feed: FDA_Inspections

> FDA inspection 1041252 of CeramTec GmbH, Medical Products Division, February 16, 2018. Classification: No Action Indicated (NAI). Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1041252
- Company Name: CeramTec GmbH, Medical Products Division
- Inspection Date: 2018-02-16
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

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- FDA Inspection 932193 - 2015-06-12
- [FDA Inspection 665629 - 2010-04-29](https://www.keypedia.com/records/fda_inspections/ceramtec-gmbh-medical-products-division/34779fc4-18a8-483a-8dd2-508c9020ae22)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/jesse-a-vazquez/cac5b170-d0ea-4355-af5d-3d81546ff0fe)

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

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