FDA Inspection 787228 — Unilever Manufacturing, Inc., U.S.

Unilever Manufacturing, Inc., U.S. — FEI 1811348

The FDA completed an inspection of Unilever Manufacturing, Inc., U.S. on Jun 20, 2012 in Huntington, IN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Food/Cosmetics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jun 20, 2012
Fiscal Year
2012
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Huntington, IN (United States)