Company
GermanyAesculap AG, Tuttlingen, Germany – FDA Inspections
Inspection records and compliance data for Aesculap AG in Tuttlingen. 8 FDA inspections on record (1 OAI), 1 Form 483, last inspected July 21, 2022.
Company Profile
This profile covers Aesculap AG based in Tuttlingen, Germany.
FDA Inspection History
- FDA inspections
- 8
- OAI
- 1
- VAI
- 0
- NAI
- 6
- Unclassified
- 1
- Form 483s
- 1
- Warning letters
- 0
First inspected June 5, 2009. Last inspected July 21, 2022.
FDA inspections (8)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| July 21, 2022 | NAI | Medical Devices & Rad Health · Compliance: Devices | 1178394 |
| June 7, 2018 | Not classified | Medical Devices & Rad Health | 1078171 |
| September 22, 2016 | NAI | Medical Devices & Rad Health · Bioresearch Monitoring | 987720 |
| July 16, 2015 | NAI | Medical Devices & Rad Health · Postmarket Assurance: Devices | 939850 |
| July 4, 2013 | NAI | Medical Devices & Rad Health · Postmarket Assurance: Devices | 841575 |
| December 4, 2012 | NAI | Medical Devices & Rad Health · Compliance: Devices | 809376 |
| May 19, 2011 | OAI | Medical Devices & Rad Health · Postmarket Assurance: Devices | 729096 |
| June 5, 2009 | NAI | Medical Devices & Rad Health · Compliance: Devices | 586922 |
FDA documents
Form 483s (1)
People (1)
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Company Information
Name
Aesculap AG
FEI Number
3002806315
Address
Am Aesculap-Platz 1, Tuttlingen, Germany
Country
Germany
ID: 7bf23acc-23fe-4733-bd67-2e0736286f2f