FDA Warning Letter — Lasik Vision Institute
The FDA took a Warning Letter action against Lasik Vision Institute on Oct 9, 2009 (Altamonte Springs, FL). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.
Action Details
- Facility
- Lasik Vision Institute
- Date
- Oct 9, 2009
- Fiscal Year
- 2010
- Product Type
- Devices
- Center
- CDRH
- Location
- Altamonte Springs, FL (United States)