FDA inspection

Akorn, Inc.: FDA inspection ending Mar 5, 2019

FDA inspection 1085157 · No Action Indicated (NAI) · Gurnee, IL

Key facts

Inspection ID 1085157
Firm Akorn, Inc.
FEI number 3003102962
Address 1925 W Field Ct Ste 300
City Gurnee
State IL
ZIP 60031
Country United States
Fiscal year 2019
Inspection end date Mar 5, 2019
Classification No Action Indicated (NAI)
Project area Bioresearch Monitoring
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
  • 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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