# FDA Inspection 1007462 - Neurotron. Inc. - April 10, 2017

Source: https://www.keypedia.com/records/fda_inspections/neurotron-inc/9041e86f-115b-42ec-99ba-3dace46b3dfd
Source feed: FDA_Inspections

> FDA Inspection 1007462 for Neurotron. Inc. on April 10, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1007462
- Company Name: Neurotron. Inc.
- Inspection Date: 2017-04-10
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1007463 - 2017-04-10](https://www.keypedia.com/records/fda_inspections/neurotron-inc/b097f5ff-ca27-4521-94ad-c27b734ea94a)
- [FDA Inspection 1007463 - 2017-04-10](https://www.keypedia.com/records/fda_inspections/neurotron-inc/d5eb77a3-b73a-45c2-8cb9-19f2eb582e13)
- [FDA Inspection 799351 - 2012-09-18](https://www.keypedia.com/records/fda_inspections/neurotron-inc/95f702e5-77d5-4970-a5eb-ab300522ef53)
- [FDA Inspection 799351 - 2012-09-18](https://www.keypedia.com/records/fda_inspections/neurotron-inc/1b165056-b8a1-4b61-82dc-d2a31c86ca9f)
- [FDA Inspection 798374 - 2012-09-12](https://www.keypedia.com/records/fda_inspections/neurotron-inc/1997fa45-7d77-4f10-986d-34ab729bbc45)

Company: https://www.keypedia.com/companies/neurotron-inc/2f572ad6-cb5f-4096-bd37-b1facb33774c

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