FDA Inspection 983647 — Core-Mark Mid-Continent, Inc.

Core-Mark Mid-Continent, Inc. — FEI 1211924

The FDA completed an inspection of Core-Mark Mid-Continent, Inc. on Sep 7, 2016 in Gardiner, ME. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Food/Cosmetics.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Sep 7, 2016
Fiscal Year
2016
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Gardiner, ME (United States)

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