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FDA Inspection 790663 — Medtronic Sofamor Danek USA Inc

Medtronic Sofamor Danek USA Inc — FEI 1000477302

The FDA completed an inspection of Medtronic Sofamor Danek USA Inc on June 6, 2012 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
June 6, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Memphis, TN (United States)

Facility

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  • 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))

FDA data resources