FDA Warning Letter — Kwik Trip

Case 524517 — FEI 3013484789

The FDA took a Warning Letter action against Kwik Trip on May 11, 2017 (Rochester, MN). The action was issued by CTP and concerns tobacco products.

Action Details

Facility
Kwik Trip
Date
May 11, 2017
Fiscal Year
2017
Product Type
Tobacco
Center
CTP
Location
Rochester, MN (United States)