FDA Inspection 901818 — Aesculap Inc
The FDA completed an inspection of Aesculap Inc on October 23, 2014 in Hazelwood, MO. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- October 23, 2014
- Fiscal Year
- 2015
- Product Type
- Biologics
- Project Area
- Human Cellular, Tissue, and Gene Therapies
- Location
- Hazelwood, MO (United States)