# Neurotron. Inc. – FDA Inspection, Aug 21, 2026

Source: https://www.keypedia.com/records/fda_inspections/neurotron-inc/f62206e1-6c2e-4186-bfd3-aff25d2435d5
Source feed: FDA_Inspections

> FDA inspection 1332018 of Neurotron. Inc., August 21, 2026. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR part 803. Form 483 issued. 6 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1332018
- Company Name: Neurotron. Inc.
- Inspection Date: 2026-08-21
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Denver District Office
- Citation Count: 6

## Related Documents

- [FDA Inspection 1007463 - 2017-04-10](https://www.keypedia.com/records/fda_inspections/neurotron-inc/d5eb77a3-b73a-45c2-8cb9-19f2eb582e13)
- [FDA Inspection 1007462 - 2017-04-10](https://www.keypedia.com/records/fda_inspections/neurotron-inc/9041e86f-115b-42ec-99ba-3dace46b3dfd)
- FDA Inspection 799351 - 2012-09-18
- FDA Inspection 798374 - 2012-09-12
- [FDA Inspection 682551 - 2010-09-27](https://www.keypedia.com/records/fda_inspections/neurotron-inc/ba0cf9a7-db26-4ed3-9eb6-06f5a9da3608)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/matthew-m-vernon/f77e8c18-8614-49e3-9b19-3327b7fe7648)

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

Office: https://www.keypedia.com/offices/denver-district-office/93b79063-390c-4759-af6c-5da7e388face