FDA Inspection 1228326 — Nuvasive PR, Inc.

Nuvasive PR, Inc. — FEI 3009144915

The FDA completed an inspection of Nuvasive PR, Inc. on January 18, 2024 in Guaynabo, PR. 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
January 18, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Guaynabo, PR (United States)