FDA Inspection 796781 — Aesculap Inc
The FDA completed an inspection of Aesculap Inc on Aug 30, 2012 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
- Aug 30, 2012
- Fiscal Year
- 2012
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Center Valley, PA (United States)