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FDA Inspection 753736 — Lightbody Medical Technologies Inc

Lightbody Medical Technologies Inc — FEI 3007048062

The FDA completed an inspection of Lightbody Medical Technologies Inc on November 2, 2011 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
November 2, 2011
Fiscal Year
2012
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