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FDA Inspection 950920 — Medtronic Sofamor Danek USA Inc

Medtronic Sofamor Danek USA Inc — FEI 1000477302

The FDA completed an inspection of Medtronic Sofamor Danek USA Inc on November 3, 2015 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
November 3, 2015
Fiscal Year
2016
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Memphis, TN (United States)

Additional Details

Sponsor, Contract Research Organization

Facility

Other inspections at this facility

  • 1302636 (NAI Fri Feb 06 2026 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 946127 (VAI Fri Oct 23 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 869386 (VAI Tue Mar 11 2014 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