FDA Warning Letter — Kwik Trip #802

Case 735621 — FEI 3046869494

The FDA took a Warning Letter action against Kwik Trip #802 on Jul 30, 2026 (Alma, WI). The action was issued by CTP and concerns tobacco products.

Action details

Facility
Kwik Trip #802
Date
Jul 30, 2026
Fiscal Year
2026
Product Type
Tobacco
Center
CTP
Location
Alma, WI (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.