# FDA Inspection 582118 - Neurotron Incorporated - May 15, 2009

Source: https://www.keypedia.com/records/fda_inspections/neurotron-incorporated/7bf9124b-7da3-4df6-aa8b-8e7b39428586
Source feed: FDA_Inspections

> FDA Inspection 582118 for Neurotron Incorporated on May 15, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 582118
- Company Name: Neurotron Incorporated
- Inspection Date: 2009-05-15
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 582118 - 2009-05-15](https://www.keypedia.com/records/fda_inspections/neurotron-incorporated/750c9d57-6a48-474c-baeb-43d0c7e674bb)

Company: https://www.keypedia.com/companies/neurotron-incorporated/3fc0e78c-add1-4afe-a911-00fe7947afe1

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