FDA Warning Letter — KELLY EXPRESS MART 53 / MOBIL

Case 519451 — FEI 3013331492

The FDA took a Warning Letter action against KELLY EXPRESS MART 53 / MOBIL on Mar 9, 2017 (Clarklake, MI). The action was issued by CTP and concerns tobacco products.

Action Details

Facility
KELLY EXPRESS MART 53 / MOBIL
Date
Mar 9, 2017
Fiscal Year
2017
Product Type
Tobacco
Center
CTP
Location
Clarklake, MI (United States)

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