FDA Inspection 901694 — Medtronic Vascular, Inc.

Medtronic Vascular, Inc. — FEI 3001452571

The FDA completed an inspection of Medtronic Vascular, Inc. on November 7, 2014 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
November 7, 2014
Fiscal Year
2015
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Santa Rosa, CA (United States)

Additional Details

Postmarket Audit Inspections