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FDA Inspection 1028734 — Stryker Neurovascular

Stryker Neurovascular — FEI 3008853977

The FDA completed an inspection of Stryker Neurovascular on October 16, 2017 in Fremont, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
October 16, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Fremont, CA (United States)

Facility

Other inspections at this facility

  • 1257117 (VAI Wed Dec 18 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1032404 (NAI Fri Sep 22 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 980716 (NAI Wed Jun 01 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 936471 (NAI Thu Jul 30 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 851608 (NAI Tue Oct 15 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources