FDA Warning Letter — Kwik Trip

Case 542878 — FEI 3014078466

The FDA took a Warning Letter action against Kwik Trip on Dec 14, 2017 (Plover, WI). The action was issued by CTP and concerns tobacco products.

Action Details

Facility
Kwik Trip
Date
Dec 14, 2017
Fiscal Year
2018
Product Type
Tobacco
Center
CTP
Location
Plover, WI (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.