# FDA Inspection 1041252 - CeramTec GmbH, Medical Products Division - February 16, 2018

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

> FDA Inspection 1041252 for CeramTec GmbH, Medical Products Division on February 16, 2018. Classification: No Action Indicated (NAI).

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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)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1041252 - 2018-02-16](https://www.globalkeysolutions.net/records/fda_inspections/ceramtec-gmbh-medical-products-division/1403bca2-5d02-490e-a0a7-86f107347fb7)
- [FDA Inspection 932193 - 2015-06-12](https://www.globalkeysolutions.net/records/fda_inspections/ceramtec-gmbh-medical-products-division/f5fdd0f2-71ac-412e-ab11-99c356d8ec9d)
- [FDA Inspection 665629 - 2010-04-29](https://www.globalkeysolutions.net/records/fda_inspections/ceramtec-gmbh-medical-products-division/0b2ef9fb-f859-447c-ae70-64f964732e13)
- [FDA Inspection 665629 - 2010-04-29](https://www.globalkeysolutions.net/records/fda_inspections/ceramtec-gmbh-medical-products-division/34779fc4-18a8-483a-8dd2-508c9020ae22)

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