FDA Warning Letter — Kwik Trip

Case 517094 — FEI 3013230828

The FDA took a Warning Letter action against Kwik Trip on Feb 9, 2017 (Mequon, WI). The action was issued by CTP and concerns tobacco products.

Action Details

Facility
Kwik Trip
Date
Feb 9, 2017
Fiscal Year
2017
Product Type
Tobacco
Center
CTP
Location
Mequon, WI (United States)

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