FDA Inspection 673762 — The Lighthouse For The Blind

The Lighthouse For The Blind — FEI 1000118065

The FDA completed an inspection of The Lighthouse For The Blind on Jul 16, 2010 in Saint Louis, MO. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jul 16, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Saint Louis, MO (United States)