FDA Inspection 1086925 — KJK Enterprise, Inc.

KJK Enterprise, Inc. — FEI 2180853

The FDA completed an inspection of KJK Enterprise, Inc. on Feb 22, 2019 in Racine, WI. 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
Feb 22, 2019
Fiscal Year
2019
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Racine, WI (United States)