FDA Inspection 704267 — Practice Medx, LLC dba BioVeda Technologies

Practice Medx, LLC dba BioVeda Technologies — FEI 3007871867

The FDA completed an inspection of Practice Medx, LLC dba BioVeda Technologies on December 2, 2010 in Boca Raton, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 2, 2010
Fiscal Year
2011
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Boca Raton, FL (United States)