FDA Warning Letter — Quik Trip

Case 535901 — FEI 3013751867

The FDA took a Warning Letter action against Quik Trip on Aug 24, 2017 (Greenville, SC). The action was issued by CTP and concerns tobacco products.

Action Details

Facility
Quik Trip
Date
Aug 24, 2017
Fiscal Year
2017
Product Type
Tobacco
Center
CTP
Location
Greenville, SC (United States)

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