FDA Inspection 1279142 — Arthrosurface, Inc.

Arthrosurface, Inc. — FEI 3004154314

The FDA completed an inspection of Arthrosurface, Inc. on August 6, 2025 in West Bridgewater, MA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 6, 2025
Fiscal Year
2025
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
West Bridgewater, MA (United States)