FDA Inspection 918977 — Remia C.V.

Remia C.V. — FEI 3009850743

The FDA completed an inspection of Remia C.V. on February 18, 2015 in Den Dolder. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 18, 2015
Fiscal Year
2015
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Den Dolder (Netherlands)

Citations

IDCFRDescription
159921 CFR 110.37(b)(5)Backflow prevention