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FDA Inspection 1155920 — NuTech Spine, Inc.

NuTech Spine, Inc. — FEI 3009169996

The FDA completed an inspection of NuTech Spine, Inc. on October 27, 2021 in Birmingham, AL. 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
October 27, 2021
Fiscal Year
2022
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Birmingham, AL (United States)

Facility

Other inspections at this facility

  • 1094097 (NAI Thu Jun 20 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1056306 (NAI Wed Apr 25 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 982009 (NAI Wed Jul 13 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 884316 (NAI Wed Jun 18 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 833696 (NAI Tue Apr 30 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources