# FDA Inspection 704267 - Practice Medx, LLC dba BioVeda Technologies - December 02, 2010

Source: https://www.keypedia.com/records/fda_inspections/practice-medx-llc-dba-bioveda-technologies/1998828d-690f-4321-8bb1-b38482e397e9
Source feed: FDA_Inspections

> FDA Inspection 704267 for Practice Medx, LLC dba BioVeda Technologies on December 02, 2010. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 704267
- Company Name: Practice Medx, LLC dba BioVeda Technologies
- Inspection Date: 2010-12-02
- Classification: No Action Indicated (NAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 704267 - 2010-12-02](https://www.keypedia.com/records/fda_inspections/practice-medx-llc-dba-bioveda-technologies/4426011a-4fea-459d-ae99-a42342ee36d5)
- [FDA Inspection 643470 - 2010-01-08](https://www.keypedia.com/records/fda_inspections/practice-medx-llc-dba-bioveda-technologies/2c79b888-c532-4fb2-9af0-4330075207b7)

Company: https://www.keypedia.com/companies/practice-medx-llc-dba-bioveda-technologies/db8e8d5b-a006-4cd8-bb70-1a4b02032907

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7