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FDA Inspection 1155286 — Stryker Spine

Stryker Spine — FEI 3004024955

The FDA completed an inspection of Stryker Spine on September 13, 2021 in Allendale, NJ. 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
September 13, 2021
Fiscal Year
2021
Product Type
Devices
Project Area
Compliance: Devices
Location
Allendale, NJ (United States)

Facility

Other inspections at this facility

  • 1251341 (NAI Fri Sep 27 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1099091 (NAI Thu Aug 01 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 965950 (NAI Fri Mar 11 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 883814 (NAI Wed Jun 18 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 763943 (NAI Thu Jan 12 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources