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FDA Inspection 845563 — Medtronic Sofamor Danek USA Inc

Medtronic Sofamor Danek USA Inc — FEI 1000477302

The FDA completed an inspection of Medtronic Sofamor Danek USA Inc on July 15, 2013 in Memphis, TN. 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
July 15, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Memphis, TN (United States)

Additional Details

Postmarket Audit Inspections

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))
  • 869386 (VAI Tue Mar 11 2014 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