FDA Inspection 837130 — Universal Pure LLC

Universal Pure LLC — FEI 3009841929

The FDA completed an inspection of Universal Pure LLC on June 20, 2013 in Meriden, CT. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 5 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 20, 2013
Fiscal Year
2013
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Meriden, CT (United States)

Citations

IDCFRDescription
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
1274921 CFR 120.8(b)(6)HACCP plan - verify procedures / frequency - none listed
1275521 CFR 120.11(a)(1)(iv)Records - not signed and dated by qualified individual
993921 CFR 120.7(c)All hazards not considered