Home / Inspections / 836180

FDA Inspection 836180 — Alphatec Spine, Inc.

Alphatec Spine, Inc. — FEI 2027467

The FDA completed an inspection of Alphatec Spine, Inc. on June 14, 2013 in Carlsbad, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
June 14, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Carlsbad, CA (United States)

Facility

Other inspections at this facility

  • 1175442 (NAI Mon Jul 18 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1020129 (NAI Wed Apr 19 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 917997 (VAI Fri Mar 13 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 779000 (VAI Fri Apr 27 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 705415 (VAI Mon Dec 13 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources