FDA inspection

Arch - MedTorque Inc.: FDA inspection ending Mar 18, 2010

FDA inspection 652628 · Voluntary Action Indicated (VAI) · Kenosha, WI

Key facts

Inspection ID 652628
Firm Arch - MedTorque Inc.
FEI number 3005874553
Address 5601 95th Ave
City Kenosha
State WI
ZIP 53144
Country United States
Fiscal year 2010
Inspection end date Mar 18, 2010
Classification Voluntary Action Indicated (VAI)
Project area Compliance: 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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