FDA Warning Letter — LCA Vision Inc/Lasik Plus Vision Center

Case 89785 — FEI 1000122789

The FDA took a Warning Letter action against LCA Vision Inc/Lasik Plus Vision Center on February 12, 2010 (Cincinnati, OH). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
LCA Vision Inc/Lasik Plus Vision Center
Date
February 12, 2010
Fiscal Year
2010
Product Type
Devices
Center
CDRH
Location
Cincinnati, OH (United States)