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FDA Inspection 746575 — AlphaProtech Incorporated

AlphaProtech Incorporated — FEI 2022409

The FDA completed an inspection of AlphaProtech Incorporated on September 14, 2011 in Nogales, AZ. 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 14, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Nogales, AZ (United States)

Facility

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FDA data resources