FDA Inspection 1311082 — SpineFrontier, Inc.

SpineFrontier, Inc. — FEI 3005977257

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

Inspection details

Classification
No Action Indicated (NAI)
End Date
Apr 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

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