FDA Inspection 752861 — NuVasive, Inc

NuVasive, Inc — FEI 3005949151

The FDA completed an inspection of NuVasive, Inc on November 9, 2011 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
November 9, 2011
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Memphis, TN (United States)