FDA Warning Letter — Quiktrip 206

Case 717372 — FEI 3039669065

The FDA took a Warning Letter action against Quiktrip 206 on September 23, 2025 (Olathe, KS). The action was issued by CTP and concerns tobacco products.

Action Details

Facility
Quiktrip 206
Date
September 23, 2025
Fiscal Year
2025
Product Type
Tobacco
Center
CTP
Location
Olathe, KS (United States)