FDA Inspection 912099 — Core-Mark Mid-Continent, Inc.

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

The FDA completed an inspection of Core-Mark Mid-Continent, Inc. on February 4, 2015 in Gardiner, ME. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Food/Cosmetics.