FDA inspection

Kirkman Group Inc: FDA inspection ending Apr 9, 2008

FDA inspection 512258 · Voluntary Action Indicated (VAI) · Lake Oswego, OR

Key facts

Inspection ID 512258
Firm Kirkman Group Inc
FEI number 3004268965
Address 6400 Rosewood St
City Lake Oswego
State OR
ZIP 97035-5392
Fiscal year 2008
Inspection end date Apr 9, 2008
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • 10–99 Citations
  • 1–9 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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