# FDA Inspection 791668 - NeuroDx Development, LLC - July 10, 2012

Source: https://www.keypedia.com/records/fda_inspections/neurodx-development-llc/8ba6b210-ffcb-4432-b136-587c8e5acaa3
Source feed: FDA_Inspections

> FDA Inspection 791668 for NeuroDx Development, LLC on July 10, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 791668
- Company Name: NeuroDx Development, LLC
- Inspection Date: 2012-07-10
- 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 988309 - 2016-06-20](https://www.keypedia.com/records/fda_inspections/neurodx-development-llc/a63198e6-5daa-4b0b-8533-eeddc9ea7761)
- [FDA Inspection 791668 - 2012-07-10](https://www.keypedia.com/records/fda_inspections/neurodx-development-llc/416e3d5f-69d9-4b1a-9c62-bd897c274994)

Company: https://www.keypedia.com/companies/neurodx-development-llc/c73a08e7-ff05-4ad7-b563-06930dff66e3

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