FDA Inspection 643470 — 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 January 8, 2010 in Boca Raton, FL. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
January 8, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Boca Raton, FL (United States)

Citations

IDCFRDescription
230221 CFR 820.20(e)Quality System Procedures
44721 CFR 820.40Lack of procedures, or not maintained