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FDA Inspection 910589 — Medtronic Navigation, Inc.

Medtronic Navigation, Inc. — FEI 1000517638

The FDA completed an inspection of Medtronic Navigation, Inc. on December 15, 2014 in Lafayette, CO. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 15, 2014
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Lafayette, CO (United States)

Facility

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Recent compliance actions

FDA data resources