FDA inspection

Core-Mark Mid-Continent, Inc.: FDA inspection ending Sep 7, 2016

FDA inspection 983647 · No Action Indicated (NAI) · Gardiner, ME

Key facts

Inspection ID 983647
Firm Core-Mark Mid-Continent, Inc.
FEI number 1211924
Address 47 Market St
City Gardiner
State ME
ZIP 04345
Country United States
Fiscal year 2016
Inspection end date Sep 7, 2016
Classification No Action Indicated (NAI)
Project area Foodborne Biological Hazards
Product type Food/Cosmetics

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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