FDA Inspection 1302434 — GFI Midwest

GFI Midwest — FEI 3012149826

The FDA completed an inspection of GFI Midwest on February 11, 2026 in Kenosha, WI. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 11, 2026
Fiscal Year
2026
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Kenosha, WI (United States)

Additional Details

FSVP

Citations

IDCFRDescription
1826321 CFR 1.504(b)(1)Hazard analysis biological, chemical, physical