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