FDA Warning Letter — Quick Mart / Kwik Mart

Case 476283 — FEI 3011702068

The FDA took a Warning Letter action against Quick Mart / Kwik Mart on Aug 13, 2015 (Baltimore, MD). The action was issued by CTP and concerns tobacco products.

Action Details

Facility
Quick Mart / Kwik Mart
Date
Aug 13, 2015
Fiscal Year
2015
Product Type
Tobacco
Center
CTP
Location
Baltimore, MD (United States)