FDA Inspection 1269758 — Directmed, Inc

Directmed, Inc — FEI 3000718659

The FDA completed an inspection of Directmed, Inc on May 15, 2025 in Glen Cove, NY. 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). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
May 15, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Glen Cove, NY (United States)

Citations

IDCFRDescription
337521 CFR 820.198(e)Records of complaint investigation
369621 CFR 820.100(b)Documentation

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