FDA Inspection 733087 — Kwik Trip, Inc.

Kwik Trip, Inc. — FEI 2127538

The FDA completed an inspection of Kwik Trip, Inc. on July 1, 2011 in La Crosse, WI. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 1, 2011
Fiscal Year
2011
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
La Crosse, WI (United States)

Citations

IDCFRDescription
130621 CFR 110.20(b)(7)Screening
168921 CFR 110.80Reasonable precautions