FDA Inspection 643172 — Aurora Products, Inc.

Aurora Products, Inc. — FEI 3002286594

The FDA completed an inspection of Aurora Products, Inc. on Jan 28, 2010 in Orange, CT. 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
Jan 28, 2010
Fiscal Year
2010
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Orange, CT (United States)