FDA Inspection 1160442 — NextPhase Medical Devices LLC

NextPhase Medical Devices LLC — FEI 3001237338

The FDA completed an inspection of NextPhase Medical Devices LLC on Jan 10, 2022 in Rochester, NH. 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). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jan 10, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
Rochester, NH (United States)

Citations

IDCFRDescription
1471021 CFR 820.150Lack of or inadequate procedures for storage.

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