FDA inspection

Medtronic Navigation, Inc.: FDA inspection ending Aug 18, 2016

FDA inspection 985377 · Voluntary Action Indicated (VAI) · Lafayette, CO

Key facts

Inspection ID 985377
Firm Medtronic Navigation, Inc.
FEI number 1000517638
Address 5927 Landau Ct
City Lafayette
State CO
ZIP 80026
Country United States
Fiscal year 2016
Inspection end date Aug 18, 2016
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: 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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