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FDA Inspection 1063130 — SpinalGraft Technologies LLC

SpinalGraft Technologies LLC — FEI 3003947416

The FDA completed an inspection of SpinalGraft Technologies LLC on June 27, 2018 in Memphis, TN. 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 27, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Memphis, TN (United States)

Facility

Other inspections at this facility

  • 1209500 (NAI Wed Jun 14 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 983086 (NAI Wed Jun 22 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 886448 (NAI Fri Jun 20 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 723698 (NAI Tue May 03 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources