FDA Inspection 977569 — Aesculap Inc
The FDA completed an inspection of Aesculap Inc on Jul 13, 2016 in Center Valley, PA. 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
- Jul 13, 2016
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Center Valley, PA (United States)