FDA Inspection 869876 — NuVasive, Inc

NuVasive, Inc — FEI 3005949151

The FDA completed an inspection of NuVasive, Inc on March 14, 2014 in Memphis, TN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 14, 2014
Fiscal Year
2014
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Memphis, TN (United States)

Citations

IDCFRDescription
1241621 CFR 1271.260(e)Storage temperatures recorded, maintained