# FDA Inspection 822069 - Brainmaster Technologies - March 05, 2013

Source: https://www.keypedia.com/records/fda_inspections/brainmaster-technologies/1c9ee508-0fe8-48b3-bc7f-250612075d4d
Source feed: FDA_Inspections

> FDA Inspection 822069 for Brainmaster Technologies on March 05, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 822069
- Company Name: Brainmaster Technologies
- Inspection Date: 2013-03-05
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: 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/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)
- [FDA Inspection 646990 - 2010-02-19](https://www.keypedia.com/records/fda_inspections/brainmaster-technologies/2e58a5dd-2f30-4d2a-a016-9c222fdd52a7)

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