FDA Inspection 1013965 — Pulsin

Pulsin — FEI 3011359272

The FDA completed an inspection of Pulsin on June 9, 2017 in Gloucester. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 9, 2017
Fiscal Year
2017
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Gloucester (United Kingdom)

Citations

IDCFRDescription
112521 CFR 110.40(a)Materials and workmanship
168921 CFR 110.80Reasonable precautions
365221 CFR 110.37(e)(1)Suitable locations