FDA Warning Letter — Kent Kwik

Case 517079 — FEI 3013232743

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

Action Details

Facility
Kent Kwik
Date
Feb 9, 2017
Fiscal Year
2017
Product Type
Tobacco
Center
CTP
Location
Midland, TX (United States)

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