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FDA Inspection 959090 — Stryker Corporation

Stryker Corporation — FEI 1811755

The FDA completed an inspection of Stryker Corporation on January 7, 2016 in Portage, MI. 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
January 7, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Portage, MI (United States)

Facility

Other inspections at this facility

  • 850254 (NAI Fri Sep 13 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 806763 (OAI Fri Nov 09 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 791489 (VAI Mon Jun 18 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 682479 (VAI Fri Sep 24 2010 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 583137 (OAI Thu May 14 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources