FDA Inspection 671376 — Arthrosurface, Inc.

Arthrosurface, Inc. — FEI 3004154314

The FDA completed an inspection of Arthrosurface, Inc. on June 11, 2010 in West Bridgewater, MA. 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
June 11, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
West Bridgewater, MA (United States)