FDA Inspection 768996 — NuVasive Inc

NuVasive Inc — FEI 3002980729

The FDA completed an inspection of NuVasive Inc on February 10, 2012 in San Diego, CA. 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 10, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
San Diego, CA (United States)

Additional Details

Sponsor, Contract Research Organization