FDA Inspection
Aesculap AGAesculap AG – FDA Inspection, Jul 21, 2022
Record Details
This FDA Inspection record concerns Aesculap AG, with an inspection on July 21, 2022, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Aesculap AG
- Inspection Date
- July 21, 2022
- Product Type
- Devices
View Company Profile
ID · c301202a-fd12-4f51-912f-3075d36b9ada
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1178394
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Aesculap AG
7| Date | Classification | Office | Project area |
|---|---|---|---|
| June 7, 2018 | Not classified | Office of Inspections and Investigations | |
| September 22, 2016 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| July 16, 2015 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| July 4, 2013 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| December 4, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Aesculap AG
- FDA Inspection 1078171 - 2018-06-07
- FDA Inspection 987720 - 2016-09-22
- FDA Inspection 939850 - 2015-07-16
- FDA Inspection 841575 - 2013-07-04
- FDA Inspection 809376 - 2012-12-04
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