FDA inspection

Midwest Compliance Laboratories, LLC: FDA inspection ending Nov 6, 2014

FDA inspection 902597 · Voluntary Action Indicated (VAI) · Terre Haute, IN

Key facts

Inspection ID 902597
Firm Midwest Compliance Laboratories, LLC
FEI number 3008429582
Address 2458 N Chamberlain St
City Terre Haute
State IN
ZIP 47805
Country United States
Fiscal year 2015
Inspection end date Nov 6, 2014
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes 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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