# Neurotron. Inc. - Inspection Records

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

> Inspection records and compliance data for Neurotron. Inc. in Aurora, Colorado. Access full analysis and detailed observations.

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## Details

- Name: Neurotron. Inc.
- FEI Number: 1121806
- City: Aurora
- State: Colorado
- Country Name: United States
- Address Line 1: 12635 E Montview Blvd Ste 127
- Zip Code: 80045

## Related Documents

- [FDA Inspection 1007462 - Neurotron. Inc. - 2017-04-10](https://www.keypedia.com/records/fda_inspections/neurotron-inc/9041e86f-115b-42ec-99ba-3dace46b3dfd) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 10, 2017
- [FDA Inspection 1007463 - Neurotron. Inc. - 2017-04-10](https://www.keypedia.com/records/fda_inspections/neurotron-inc/b097f5ff-ca27-4521-94ad-c27b734ea94a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 10, 2017
- [FDA Inspection 1007463 - Neurotron. Inc. - 2017-04-10](https://www.keypedia.com/records/fda_inspections/neurotron-inc/d5eb77a3-b73a-45c2-8cb9-19f2eb582e13) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 10, 2017
- [FDA Inspection 799351 - Neurotron. Inc. - 2012-09-18](https://www.keypedia.com/records/fda_inspections/neurotron-inc/1b165056-b8a1-4b61-82dc-d2a31c86ca9f) — classification: No Action Indicated (NAI), source: FDA, date: September 18, 2012
- [FDA Inspection 799351 - Neurotron. Inc. - 2012-09-18](https://www.keypedia.com/records/fda_inspections/neurotron-inc/95f702e5-77d5-4970-a5eb-ab300522ef53) — classification: No Action Indicated (NAI), source: FDA, date: September 18, 2012
- [FDA Inspection 798374 - Neurotron. Inc. - 2012-09-12](https://www.keypedia.com/records/fda_inspections/neurotron-inc/7446c8b0-2451-4ecd-b4b8-608c7653089d) — classification: No Action Indicated (NAI), source: FDA, date: September 12, 2012
- [FDA Inspection 798374 - Neurotron. Inc. - 2012-09-12](https://www.keypedia.com/records/fda_inspections/neurotron-inc/1997fa45-7d77-4f10-986d-34ab729bbc45) — classification: No Action Indicated (NAI), source: FDA, date: September 12, 2012
- [FDA Inspection 682551 - Neurotron. Inc. - 2010-09-27](https://www.keypedia.com/records/fda_inspections/neurotron-inc/82f5ce22-1580-4528-ba0e-ef473977dbca) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 27, 2010
- [FDA Inspection 682551 - Neurotron. Inc. - 2010-09-27](https://www.keypedia.com/records/fda_inspections/neurotron-inc/ba0cf9a7-db26-4ed3-9eb6-06f5a9da3608) — classification: No Action Indicated (NAI), source: FDA, date: September 27, 2010
- [FDA Inspection 554398 - Neurotron. Inc. - 2008-12-17](https://www.keypedia.com/records/fda_inspections/neurotron-inc/e6adeb7e-6141-4fc5-a653-bf15c837b75d) — classification: No Action Indicated (NAI), source: FDA, date: December 17, 2008

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