FDA Warning Letter — LasikPlus Vision Center

Case 255515 — FEI 3009161148

The FDA took a Warning Letter action against LasikPlus Vision Center on April 3, 2012 (Atlanta, GA). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
LasikPlus Vision Center
Date
April 3, 2012
Fiscal Year
2012
Product Type
Devices
Center
CDRH
Location
Atlanta, GA (United States)