FDA Inspection 986649 — Aesculap Inc
The FDA completed an inspection of Aesculap Inc on September 14, 2016 in Hazelwood, MO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- September 14, 2016
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Hazelwood, MO (United States)
Additional Details
Postmarket Audit Inspections