FDA Inspection 995266 — Kwik Trip, Inc.

Kwik Trip, Inc. — FEI 2127538

The FDA completed an inspection of Kwik Trip, Inc. on November 23, 2016 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
November 23, 2016
Fiscal Year
2017
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
La Crosse, WI (United States)

Citations

IDCFRDescription
1813821 CFR 117.10Personnel
1814221 CFR 117.35(a)Sanitary operations - Plant sanitation