FDA Inspection 1311082 — SpineFrontier, Inc.

SpineFrontier, Inc. — FEI 3005977257

The FDA completed an inspection of SpineFrontier, Inc. on April 2, 2026 in Burlington, MA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
April 2, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Burlington, MA (United States)

Citations

IDCFRDescription
23259ISO 13485:2016 Clause 8.5.2Corrective action records not maintained