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FDA Inspection 844341 — SpineFrontier, Inc.

SpineFrontier, Inc. — FEI 3005977257

The FDA completed an inspection of SpineFrontier, Inc. on August 5, 2013 in Burlington, MA. 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 5, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Burlington, MA (United States)

Facility

Other inspections at this facility

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  • 1078558 (NAI Tue Jan 29 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1036897 (NAI Wed Nov 29 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 960829 (NAI Wed Feb 10 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 791636 (OAI Wed Jul 11 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources