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FDA Inspection 746838 — NextPhase Medical Devices LLC

NextPhase Medical Devices LLC — FEI 3003174284

The FDA completed an inspection of NextPhase Medical Devices LLC on September 26, 2011 in Mansfield, MA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 26, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Mansfield, MA (United States)

Facility

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FDA data resources