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FDA Inspection 855281 — Medtronic Vascular, Inc.

Medtronic Vascular, Inc. — FEI 3001452571

The FDA completed an inspection of Medtronic Vascular, Inc. on November 14, 2013 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 14, 2013
Fiscal Year
2014
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Santa Rosa, CA (United States)

Facility

Other inspections at this facility

  • 1096966 (NAI Thu Jul 11 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1030899 (NAI Thu Aug 31 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 901694 (NAI Fri Nov 07 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 819376 (NAI Fri Feb 22 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 810454 (VAI Tue Nov 27 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources