FDA inspection

Antares Pharma, Inc.: FDA inspection ending Jul 14, 2009

FDA inspection 596396 · No Action Indicated (NAI) · Minnetonka, MN

Key facts

Inspection ID 596396
Firm Antares Pharma, Inc.
FEI number 2182861
Address 12500 Whitewater Dr
City Minnetonka
State MN
ZIP 55343
Country United States
Fiscal year 2009
Inspection end date Jul 14, 2009
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

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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