FDA Inspection
CeramTec GmbH, Medical Products DivisionCeramTec GmbH, Medical Products Division – FDA Inspection, Feb 16, 2018
Record Details
This FDA Inspection record concerns CeramTec GmbH, Medical Products Division, with an inspection on February 16, 2018, issued by the Center for Devices and Radiological Health, covering devices.
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ID · d0d6fb89-4ccc-4b48-931a-04a756d6607e
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1041252
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
- Outcome
- Form 483 issued
Other FDA inspections of CeramTec GmbH, Medical Products Division
3| Date | Classification | Office | Project area |
|---|---|---|---|
| January 19, 2023 | Not classified | Office of Inspections and Investigations | |
| June 12, 2015 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| April 29, 2010 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for CeramTec GmbH, Medical Products Division
- FDA Inspection 1197933 - 2023-01-19
- FDA Inspection 932193 - 2015-06-12
- FDA Inspection 665629 - 2010-04-29
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