FDA Inspection 782683 — Gudrun Group N.V.

Gudrun Group N.V. — FEI 3004276547

The FDA completed an inspection of Gudrun Group N.V. on May 4, 2012 in Lier. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
May 4, 2012
Fiscal Year
2012
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Lier (Belgium)