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FDA Inspection 917203 — Medtronic Heart Valves Division

Medtronic Heart Valves Division — FEI 2025587

The FDA completed an inspection of Medtronic Heart Valves Division on March 9, 2015 in Santa Ana, 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
March 9, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Santa Ana, CA (United States)

Facility

Other inspections at this facility

  • 1131979 (VAI Mon Oct 26 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 965285 (VAI Wed Mar 30 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 870529 (NAI Fri Mar 07 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 850644 (NAI Tue Sep 03 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 669393 (VAI Thu Jun 24 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources