FDA inspection

Akorn, Inc.: FDA inspection ending Jul 28, 2006

FDA inspection 435954 · No Action Indicated (NAI) · Lake Forest, IL

Key facts

Inspection ID 435954
Firm Akorn, Inc.
FEI number 3003102962
Address 1925 W Field Ct Ste 300
City Lake Forest
State IL
ZIP 60045-4862
Fiscal year 2006
Inspection end date Jul 28, 2006
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
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 10–99 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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