FDA Inspection 885327 — NuVasive, Inc

NuVasive, Inc — FEI 3005949151

The FDA completed an inspection of NuVasive, Inc on June 26, 2014 in Memphis, TN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
June 26, 2014
Fiscal Year
2014
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Memphis, TN (United States)