FDA Warning Letter — LasikPlus Vision Center
The FDA took a Warning Letter action against LasikPlus Vision Center on Oct 9, 2009 (Indianapolis, IN). 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
- Oct 9, 2009
- Fiscal Year
- 2010
- Product Type
- Devices
- Center
- CDRH
- Location
- Indianapolis, IN (United States)