FDA Inspection 787390 — DePuy Spine, Inc.

DePuy Spine, Inc. — FEI 1526439

The FDA completed an inspection of DePuy Spine, Inc. on June 11, 2012 in Raynham, 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, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Raynham, MA (United States)