FDA Warning Letter — KMART

Case 512348 — FEI 3013030715

The FDA took a Warning Letter action against KMART on Dec 8, 2016 (Mishawaka, IN). The action was issued by CTP and concerns tobacco products.

Action Details

Facility
KMART
Date
Dec 8, 2016
Fiscal Year
2017
Product Type
Tobacco
Center
CTP
Location
Mishawaka, IN (United States)