FDA Inspection 882771 — Myllan-ORA ehf

Myllan-ORA ehf — FEI 3001017171

The FDA completed an inspection of Myllan-ORA ehf on May 13, 2014 in Kopavogur. 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
May 13, 2014
Fiscal Year
2014
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Kopavogur (Iceland)

Citations

IDCFRDescription
451621 CFR 108.35(c)(2)(i)Limited process filing