FDA inspection

Intertek Champaign Labratory: FDA inspection ending Mar 5, 2015

FDA inspection 916715 · No Action Indicated (NAI) · Champaign, IL

Key facts

Inspection ID 916715
Firm Intertek Champaign Labratory
FEI number 3003179500
Address 711 Parkland Ct
City Champaign
State IL
ZIP 61821
Country United States
Fiscal year 2015
Inspection end date Mar 5, 2015
Classification No Action Indicated (NAI)
Project area Drug Quality Assurance
Product type Drugs

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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