FDA Inspection 901818 — Aesculap Inc
The FDA completed an inspection of Aesculap Inc on Oct 23, 2014 in Hazelwood, MO. 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
- Oct 23, 2014
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Hazelwood, MO (United States)