FDA Inspection 1157183 — Hampton Medical Devices, LLC

Hampton Medical Devices, LLC — FEI 1937445

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)