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FDA Inspection 869386 — Medtronic Sofamor Danek USA Inc

Medtronic Sofamor Danek USA Inc — FEI 1000477302

The FDA completed an inspection of Medtronic Sofamor Danek USA Inc on March 11, 2014 in Memphis, TN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 11, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Memphis, TN (United States)

Facility

Other inspections at this facility

  • 1302636 (NAI Fri Feb 06 2026 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 950920 (VAI Tue Nov 03 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 946127 (VAI Fri Oct 23 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 845563 (NAI Mon Jul 15 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 790663 (NAI Wed Jun 06 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources