FDA Inspection 1055539 — Aesculap Inc
The FDA completed an inspection of Aesculap Inc on Jun 13, 2018 in Hazelwood, MO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Jun 13, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Hazelwood, MO (United States)