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FDA Inspection 981779 — Stryker Corporation

Stryker Corporation — FEI 2936485

The FDA completed an inspection of Stryker Corporation on August 25, 2016 in San Jose, CA. 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
August 25, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
San Jose, CA (United States)

Facility

Other inspections at this facility

  • 1110636 (VAI Thu Nov 21 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 943626 (NAI Fri Sep 18 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 896766 (VAI Wed Oct 08 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 772257 (VAI Wed Mar 14 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 716353 (VAI Tue Mar 22 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources