# FDA Inspection 554322 - Neurodyne Medical Corporation - November 13, 2008

Source: https://www.keypedia.com/records/fda_inspections/neurodyne-medical-corporation/3c9c5225-ded6-4f04-bdcd-ac8fc09f0045
Source feed: FDA_Inspections

> FDA Inspection 554322 for Neurodyne Medical Corporation on November 13, 2008. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 554322
- Company Name: Neurodyne Medical Corporation
- Inspection Date: 2008-11-13
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 754792 - 2011-12-02](https://www.keypedia.com/records/fda_inspections/neurodyne-medical-corporation/77212ab3-84dc-4f2b-8ff0-e4ffc0377bee)

Company: https://www.keypedia.com/companies/neurodyne-medical-corporation/c56b3892-ccbe-4842-9e74-6c38c8859dd7

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