FDA Inspection 1229391 — NuVasive, Inc

NuVasive, Inc — FEI 3005949151

The FDA completed an inspection of NuVasive, Inc on January 30, 2024 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
January 30, 2024
Fiscal Year
2024
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Memphis, TN (United States)