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