FDA inspection

Allina Health [IRB]: FDA inspection ending Feb 11, 2000

FDA inspection 13559 · Voluntary Action Indicated (VAI) · Minneapolis, MN

Key facts

Inspection ID 13559
Firm Allina Health [IRB]
FEI number 3003062780
Address 2925 Chicago Ave
City Minneapolis
State MN
ZIP 55407-1321
Fiscal year 2000
Inspection end date Feb 11, 2000
Classification Voluntary Action Indicated (VAI)
Project area Product Evaluation: Med Devices
Product type Devices

At a glance

  • None 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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