FDA Warning Letter — Kwik Trip

Case 518665 — FEI 3013306128

The FDA took a Warning Letter action against Kwik Trip on Mar 2, 2017 (Sheboygan, WI). The action was issued by CTP and concerns tobacco products.

Action Details

Facility
Kwik Trip
Date
Mar 2, 2017
Fiscal Year
2017
Product Type
Tobacco
Center
CTP
Location
Sheboygan, WI (United States)

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