FDA inspection

Intricon Corp: FDA inspection ending Mar 15, 2005

FDA inspection 371004 · Voluntary Action Indicated (VAI) · Arden Hills, MN

Key facts

Inspection ID 371004
Firm Intricon Corp
FEI number 3003007876
Address 1260 Red Fox Rd
City Arden Hills
State MN
ZIP 55112-6944
Fiscal year 2005
Inspection end date Mar 15, 2005
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Med Devices
Product type Devices

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes 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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