FDA Inspection 1009401 — Medtronic Vascular, Inc.

Medtronic Vascular, Inc. — FEI 3008493192

The FDA completed an inspection of Medtronic Vascular, Inc. on April 19, 2017 in Sunnyvale, CA. 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
April 19, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Sunnyvale, CA (United States)