# FDA Inspection 646990 - Brainmaster Technologies - February 19, 2010

Source: https://www.keypedia.com/records/fda_inspections/brainmaster-technologies/2e58a5dd-2f30-4d2a-a016-9c222fdd52a7
Source feed: FDA_Inspections

> FDA Inspection 646990 for Brainmaster Technologies on February 19, 2010. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 646990
- Company Name: Brainmaster Technologies
- Inspection Date: 2010-02-19
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 822069 - 2013-03-05](https://www.keypedia.com/records/fda_inspections/brainmaster-technologies/1c9ee508-0fe8-48b3-bc7f-250612075d4d)
- [FDA Inspection 822069 - 2013-03-05](https://www.keypedia.com/records/fda_inspections/brainmaster-technologies/73e41484-54b4-47c4-b071-d627d944aa38)
- [FDA Inspection 646990 - 2010-02-19](https://www.keypedia.com/records/fda_inspections/brainmaster-technologies/0348681c-3a4d-45d9-896a-bf05f0349934)

Company: https://www.keypedia.com/companies/brainmaster-technologies/f52eea4e-bcfb-4985-a781-bd1ceda339d6

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