FDA Warning Letter — Practice Medx, LLC dba BioVeda Technologies

Case 101225 — FEI 3007871867

The FDA took a Warning Letter action against Practice Medx, LLC dba BioVeda Technologies on August 5, 2010 (Boca Raton, FL). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Practice Medx, LLC dba BioVeda Technologies
Date
August 5, 2010
Fiscal Year
2010
Product Type
Devices
Center
CDRH
Location
Boca Raton, FL (United States)