FDA Inspection 671376 — Arthrosurface, Inc.

Arthrosurface, Inc. — FEI 3004154314

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

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