FDA Inspection
Aesculap AGAesculap AG – FDA Inspection, May 19, 2011
Record Details
This FDA Inspection record concerns Aesculap AG, with an inspection on May 19, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Aesculap AG
- Inspection Date
- May 19, 2011
- Product Type
- Devices
View Company Profile
ID · 82a8b036-6293-4bf3-8ef0-4d677828f993
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 729096
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of Aesculap AG
7| Date | Classification | Office | Project area |
|---|---|---|---|
| July 21, 2022 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| 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 |
Other documents for Aesculap AG
- FDA Inspection 1178394 - 2022-07-21
- FDA Inspection 1078171 - 2018-06-07
- FDA Inspection 987720 - 2016-09-22
- FDA Inspection 939850 - 2015-07-16
- FDA Inspection 841575 - 2013-07-04
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