FDA Inspection 1116395 — Kwik Trip

Kwik Trip — FEI 3015691782

The FDA completed an inspection of Kwik Trip on January 2, 2020 in Byron, MN. 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
January 2, 2020
Fiscal Year
2020
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Byron, MN (United States)