FDA Inspection 1157183 — Hampton Medical Devices, LLC
The FDA completed an inspection of Hampton Medical Devices, LLC on Nov 8, 2021 in Festus, 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
- Nov 8, 2021
- Fiscal Year
- 2022
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Festus, MO (United States)