FDA Inspection 968311 — Medtronic Vascular, Inc.

Medtronic Vascular, Inc. — FEI 3005364322

The FDA completed an inspection of Medtronic Vascular, Inc. on January 21, 2016 in Santa Rosa, 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
January 21, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Santa Rosa, CA (United States)