FDA Inspection 1167317 — SI-BONE, Inc.

SI-BONE, Inc. — FEI 3007700286

The FDA completed an inspection of SI-BONE, Inc. on Mar 31, 2022 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
Mar 31, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
Santa Clara, CA (United States)