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FDA Inspection 621844 — Medtronic Sofamor Danek USA Inc

Medtronic Sofamor Danek USA Inc — FEI 1000477302

The FDA completed an inspection of Medtronic Sofamor Danek USA Inc on October 6, 2009 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
October 6, 2009
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Memphis, TN (United States)

Facility

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FDA data resources