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FDA Inspection 1020183 — Universal Pure LLC

Universal Pure LLC — FEI 3009841929

The FDA completed an inspection of Universal Pure LLC on August 3, 2017 in Meriden, CT. 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
August 3, 2017
Fiscal Year
2017
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Meriden, CT (United States)

Facility

Other inspections at this facility

  • 1125753 (VAI Tue Jul 21 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1099858 (VAI Wed Aug 14 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 981490 (OAI Fri Aug 12 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 837130 (NAI Thu Jun 20 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources