FDA Inspection 1214534 — SPINE INNOVATION, LLC

SPINE INNOVATION, LLC — FEI 3013393446

The FDA completed an inspection of SPINE INNOVATION, LLC on July 20, 2023 in Del Mar, CA. 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
July 20, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Del Mar, CA (United States)