FDA Inspection 1133262 — Core-Mark Mid-Continent, Inc.

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

The FDA completed an inspection of Core-Mark Mid-Continent, Inc. on Nov 4, 2020 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
Nov 4, 2020
Fiscal Year
2021
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.