FDA Warning Letter — Double Kwik/BP

Case 509531 — FEI 3012829836

The FDA took a Warning Letter action against Double Kwik/BP on Oct 27, 2016 (Pikeville, KY). The action was issued by CTP and concerns tobacco products.

Action details

Facility
Double Kwik/BP
Date
Oct 27, 2016
Fiscal Year
2017
Product Type
Tobacco
Center
CTP
Location
Pikeville, KY (United States)

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