FDA Inspection
CeramTec GmbH, Medical Products DivisionCeramTec GmbH, Medical Products Division – FDA Inspection, Feb 9, 2012
Record Details
This FDA Inspection record concerns CeramTec GmbH, Medical Products Division, with an inspection on February 9, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- February 9, 2012
- Product Type
- Devices
View Company Profile
ID · fc13c4b9-7471-4e1e-a589-f0624617a7d5
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 773131
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of CeramTec GmbH, Medical Products Division
3| Date | Classification | Office | Project area |
|---|---|---|---|
| February 9, 2023 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| February 14, 2018 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| June 10, 2015 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for CeramTec GmbH, Medical Products Division
- FDA Inspection 1198717 - 2023-02-09
- FDA Inspection 1041074 - 2018-02-14
- FDA Inspection 932190 - 2015-06-10
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.