FDA Inspection 1276382 — Si-Bone, Inc.

Si-Bone, Inc. — FEI 3021948057

The FDA completed an inspection of Si-Bone, Inc. on Jun 12, 2025 in Santa Clara, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jun 12, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Santa Clara, CA (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.