FDA Inspection 1073567 — Hampton Medical Devices, LLC

Hampton Medical Devices, LLC — FEI 1937445

The FDA completed an inspection of Hampton Medical Devices, LLC on Dec 3, 2018 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.