FDA inspection

Medtronic Vascular, Inc.: FDA inspection ending Nov 20, 2009

FDA inspection 637813 · Voluntary Action Indicated (VAI) · Santa Rosa, CA

Key facts

Inspection ID 637813
Firm Medtronic Vascular, Inc.
FEI number 3001452571
Address 3576 Unocal Pl
City Santa Rosa
State CA
ZIP 95403
Country United States
Fiscal year 2010
Inspection end date Nov 20, 2009
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: 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
  • 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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