FDA Warning Letter — Kwik Trip

Case 542042 — FEI 3014014309

The FDA took a Warning Letter action against Kwik Trip on Nov 30, 2017 (Sheboygan, WI). The action was issued by CTP and concerns tobacco products.

Action Details

Facility
Kwik Trip
Date
Nov 30, 2017
Fiscal Year
2018
Product Type
Tobacco
Center
CTP
Location
Sheboygan, WI (United States)

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