FDA Inspection 1096966 — Medtronic Vascular, Inc.

Medtronic Vascular, Inc. — FEI 3001452571

The FDA completed an inspection of Medtronic Vascular, Inc. on July 11, 2019 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
July 11, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Santa Rosa, CA (United States)