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FDA Inspection 651661 — Medtronic Sofamor Danek USA Inc

Medtronic Sofamor Danek USA Inc — FEI 1000477302

The FDA completed an inspection of Medtronic Sofamor Danek USA Inc on March 4, 2010 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
March 4, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Memphis, TN (United States)

Additional Details

Sponsor, Contract Research Organization

Facility

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FDA data resources