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FDA Inspection 976758 — Medtronic Vascular, Inc.

Medtronic Vascular, Inc. — FEI 3005364322

The FDA completed an inspection of Medtronic Vascular, Inc. on April 19, 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
April 19, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Santa Rosa, CA (United States)

Facility

Other inspections at this facility

  • 1026763 (NAI Fri Sep 08 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 968311 (NAI Thu Jan 21 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 841494 (VAI Wed Sep 04 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 595178 (NAI Fri Jun 19 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources