FDA Warning Letter — Kwik Mart/Shell

Case 513884 — FEI 3013089417

The FDA took a Warning Letter action against Kwik Mart/Shell on Dec 22, 2016 (Indianapolis, IN). The action was issued by CTP and concerns tobacco products.

Action Details

Facility
Kwik Mart/Shell
Date
Dec 22, 2016
Fiscal Year
2017
Product Type
Tobacco
Center
CTP
Location
Indianapolis, IN (United States)