FDA Inspection 1279419 — Subchondral Solutions, Inc.

Subchondral Solutions, Inc. — FEI 3016660811

The FDA completed an inspection of Subchondral Solutions, Inc. on July 24, 2025 in Huntington Beach, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
July 24, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Huntington Beach, CA (United States)