FDA Warning Letter — 20/20 Institute
The FDA took a Warning Letter action against 20/20 Institute on December 18, 2012 (Indianapolis, IN). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.
Action Details
- Facility
- 20/20 Institute
- Date
- December 18, 2012
- Fiscal Year
- 2013
- Product Type
- Devices
- Center
- CDRH
- Location
- Indianapolis, IN (United States)