# FDA Inspection 971930 - Neurotron Medical Inc. - November 23, 2015

Source: https://www.keypedia.com/records/fda_inspections/neurotron-medical-inc/3a3af0da-d3fb-4dbb-9e3c-03b5a7df10c4
Source feed: FDA_Inspections

> FDA Inspection 971930 for Neurotron Medical Inc. on November 23, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 971930
- Company Name: Neurotron Medical Inc.
- Inspection Date: 2015-11-23
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 778084 - 2012-04-27](https://www.keypedia.com/records/fda_inspections/neurotron-medical-inc/5d630e72-49fe-4314-a921-05ce00324fe3)
- [FDA Inspection 778084 - 2012-04-27](https://www.keypedia.com/records/fda_inspections/neurotron-medical-inc/80c7fb67-e6e3-4cdc-98ac-a4b5270e4a13)
- [FDA Inspection 563969 - 2009-02-23](https://www.keypedia.com/records/fda_inspections/neurotron-medical-inc/afc418cd-19f0-4db8-a4b5-67126e7160eb)
- [FDA Inspection 563969 - 2009-02-23](https://www.keypedia.com/records/fda_inspections/neurotron-medical-inc/245fb9a4-f330-4070-b39f-0fb53d91c6d7)

Company: https://www.keypedia.com/companies/neurotron-medical-inc/cd8284f1-104b-48f5-aa72-392469492da6

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