FDA Inspection 1279419 — Subchondral Solutions, Inc.

Subchondral Solutions, Inc. — FEI 3016660811

The FDA completed an inspection of Subchondral Solutions, Inc. on Jul 24, 2025 in Costa Mesa, 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
Jul 24, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Costa Mesa, CA (United States)

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