FDA Inspection 697682 — Interpac Technologies, Inc.

Interpac Technologies, Inc. — FEI 2935764

The FDA completed an inspection of Interpac Technologies, Inc. on November 9, 2010 in Woodland, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
November 9, 2010
Fiscal Year
2011
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Woodland, CA (United States)