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FDA Inspection 649964 — Medtronic Sofamor Danek USA Inc

Medtronic Sofamor Danek USA Inc — FEI 1000477302

The FDA completed an inspection of Medtronic Sofamor Danek USA Inc on February 25, 2010 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
February 25, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Memphis, TN (United States)

Facility

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FDA data resources