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FDA Inspection 1011653 — Amerilab Technologies, Inc

Amerilab Technologies, Inc — FEI 3000206080

The FDA completed an inspection of Amerilab Technologies, Inc on April 17, 2017 in Plymouth, MN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
April 17, 2017
Fiscal Year
2017
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Plymouth, MN (United States)

Facility

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  • 1149887 (NAI Wed Aug 18 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 871240 (NAI Thu Mar 20 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 870733 (NAI Thu Mar 20 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 778185 (NAI Mon Apr 23 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources