FDA Inspection
Aesculap AGAesculap AG – FDA Inspection, Jun 7, 2018
Record Details
This FDA Inspection record concerns Aesculap AG, with an inspection on June 7, 2018, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
- Company
- Aesculap AG
- Inspection Date
- June 7, 2018
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · 9df33de5-3680-487a-ac21-a07699d6e643
Inspection Facts
- Inspection number
- 1078171
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of Aesculap AG
7| Date | Classification | Office | Project area |
|---|---|---|---|
| July 21, 2022 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| 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 1178394 - 2022-07-21
- 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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