FDA Inspection 829006 — Kwik Trip, Inc.

Kwik Trip, Inc. — FEI 2130407

The FDA completed an inspection of Kwik Trip, Inc. on April 12, 2013 in La Crosse, WI. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Food/Cosmetics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
April 12, 2013
Fiscal Year
2013
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
La Crosse, WI (United States)