FDA Inspection 591740 — LCA Vision Inc/Lasik Plus Vision Center

LCA Vision Inc/Lasik Plus Vision Center — FEI 1000122789

The FDA completed an inspection of LCA Vision Inc/Lasik Plus Vision Center on August 5, 2009 in Cincinnati, 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
August 5, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Cincinnati, OH (United States)