FDA inspection

Intertek Champaign Labratory: FDA inspection ending Sep 30, 2010

FDA inspection 681945 · Voluntary Action Indicated (VAI) · Champaign, IL

Key facts

Inspection ID 681945
Firm Intertek Champaign Labratory
FEI number 3003179500
Address 711 Parkland Ct
City Champaign
State IL
ZIP 61821
Country United States
Fiscal year 2010
Inspection end date Sep 30, 2010
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • None 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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