FDA Inspection 1120583 — NuVasive, Inc

NuVasive, Inc — FEI 3005949151

The FDA completed an inspection of NuVasive, Inc on February 7, 2020 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
February 7, 2020
Fiscal Year
2020
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Memphis, TN (United States)