FDA Inspection 751402 — Aesculap Inc
The FDA completed an inspection of Aesculap Inc on October 17, 2011 in Center Valley, PA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- October 17, 2011
- Fiscal Year
- 2012
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Center Valley, PA (United States)