Home / Inspections / 1093586

FDA Inspection 1093586 — Lightbody Medical Technologies Inc

Lightbody Medical Technologies Inc — FEI 3007048062

The FDA completed an inspection of Lightbody Medical Technologies Inc on June 4, 2019 in Burr Ridge, IL. 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 4, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Burr Ridge, IL (United States)

Facility

Other inspections at this facility

  • 1279663 (VAI Wed Aug 27 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 981339 (NAI Mon Aug 22 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 889069 (NAI Thu Jul 24 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 753736 (NAI Wed Nov 02 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 592915 (NAI Wed Jun 17 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources