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FDA Inspection 592915 — Lightbody Medical Technologies Inc

Lightbody Medical Technologies Inc — FEI 3007048062

The FDA completed an inspection of Lightbody Medical Technologies Inc on June 17, 2009 in Burr Ridge, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
June 17, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Burr Ridge, IL (United States)

Facility

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FDA data resources