FDA Warning Letter — Kwik Trip

Case 539425 — FEI 3013898314

The FDA took a Warning Letter action against Kwik Trip on Oct 19, 2017 (Greenwood, WI). The action was issued by CTP and concerns tobacco products.

Action Details

Facility
Kwik Trip
Date
Oct 19, 2017
Fiscal Year
2018
Product Type
Tobacco
Center
CTP
Location
Greenwood, WI (United States)

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