FDA inspection

Medtronic Navigation, Inc.: FDA inspection ending Feb 19, 2014

FDA inspection 868471 · Voluntary Action Indicated (VAI) · Lafayette, CO

Key facts

Inspection ID 868471
Firm Medtronic Navigation, Inc.
FEI number 1000517638
Address 826 Coal Creek Cir
City Lafayette
State CO
ZIP 80026
Country United States
Fiscal year 2014
Inspection end date Feb 19, 2014
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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