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FDA Inspection 981339 — Lightbody Medical Technologies Inc

Lightbody Medical Technologies Inc — FEI 3007048062

The FDA completed an inspection of Lightbody Medical Technologies Inc on August 22, 2016 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
August 22, 2016
Fiscal Year
2016
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Burr Ridge, IL (United States)

Facility

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FDA data resources