FDA Inspection 987720 — Aesculap AG
The FDA completed an inspection of Aesculap AG on Sep 22, 2016 in Tuttlingen. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Sep 22, 2016
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Project Evaluation: Devices
- Location
- Tuttlingen (Germany)
Additional Details
Postmarket Audit Inspections