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FDA Inspection 1090256 — DePuy Spine, Inc.

DePuy Spine, Inc. — FEI 1526439

The FDA completed an inspection of DePuy Spine, Inc. on April 18, 2019 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
April 18, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Raynham, MA (United States)

Facility

Other inspections at this facility

  • 1021012 (NAI Fri Jun 16 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 787390 (NAI Mon Jun 11 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 767079 (VAI Fri Feb 10 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 580522 (VAI Tue Apr 28 2009 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 577762 (NAI Tue Apr 21 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources