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FDA Inspection 805149 — NuVasive Inc

NuVasive Inc — FEI 3002980729

The FDA completed an inspection of NuVasive Inc on November 2, 2012 in San Diego, CA. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
November 2, 2012
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
San Diego, CA (United States)

Facility

Other inspections at this facility

  • 1011810 (NAI Fri May 26 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 904804 (NAI Wed Nov 19 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 865024 (NAI Wed Feb 05 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 768996 (NAI Fri Feb 10 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 729198 (NAI Fri Jun 17 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources