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FDA Inspection
•Medtronic Navigation, Inc.•March 24, 2011

Medtronic Navigation, Inc. – FDA Inspection, Mar 24, 2011

Record Details

This FDA Inspection record concerns Medtronic Navigation, Inc., with an inspection on March 24, 2011, issued by the Center for Devices and Radiological Health, covering devices.

Company
Medtronic Navigation, Inc.
Inspection Date
March 24, 2011
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 2ff46971-69a1-4283-8ce0-008241ac5f87

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
715960
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

FDA Citations

1
  1. 21 CFR 820.100(b)Documentation

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Medtronic Navigation, Inc.

14
DateClassificationOfficeProject area
August 27, 2025Not classifiedDenver District Office
February 9, 2024NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
June 29, 2021VAICenter for Devices and Radiological HealthCompliance: Devices
September 30, 2019VAICenter for Devices and Radiological HealthRadiation Control and Health Safety Act
August 2, 2018Not classifiedDenver District Office
View all 14 other inspections on the company page
Other documents for Medtronic Navigation, Inc.
  • FDA Inspection 1287072 - 2025-08-27
  • FDA Inspection 1231178 - 2024-02-09
  • FDA Inspection 1145034 - 2021-06-29
  • FDA Inspection 1103549 - 2019-09-30
  • FDA Inspection 1106068 - 2018-08-02

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