FDA Inspection 1099858 — Universal Pure LLC

Universal Pure LLC — FEI 3009841929

The FDA completed an inspection of Universal Pure LLC on August 14, 2019 in Meriden, CT. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 4 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 14, 2019
Fiscal Year
2019
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Meriden, CT (United States)

Citations

IDCFRDescription
1273221 CFR 120.10(a)Corrective action - predetermined plan
1274621 CFR 120.8(b)(2)HACCP plan - critical control points not listed
1274821 CFR 120.8(b)(5)HACCP plan - corrective action plan not included
1275021 CFR 120.8(b)(6)HACCP plan - valid procedures / frequency - none listed