FDA Inspection 616925 — LASIK Vision Institute LLC

LASIK Vision Institute LLC — FEI 3007692135

The FDA completed an inspection of LASIK Vision Institute LLC on July 9, 2009 in West Chester, OH. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
July 9, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
West Chester, OH (United States)