# Neurotron. Inc., Aurora, CO – FDA Inspections

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

> Inspection records and compliance data for Neurotron. Inc. in Aurora, Colorado. 6 FDA inspections on record, 2 Form 483s, last inspected April 10, 2017.

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## Details

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

## Related Documents

- FDA Inspection 1007463 - Neurotron. Inc. - 2017-04-10 — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 10, 2017
- [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/d5eb77a3-b73a-45c2-8cb9-19f2eb582e13) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 10, 2017
- FDA Inspection 799351 - Neurotron. Inc. - 2012-09-18 — classification: No Action Indicated (NAI), source: FDA, date: September 18, 2012
- FDA Inspection 799351 - Neurotron. Inc. - 2012-09-18 — classification: No Action Indicated (NAI), source: FDA, date: September 18, 2012
- FDA Inspection 798374 - Neurotron. Inc. - 2012-09-12 — classification: No Action Indicated (NAI), source: FDA, date: September 12, 2012
- FDA Inspection 798374 - Neurotron. Inc. - 2012-09-12 — 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/ba0cf9a7-db26-4ed3-9eb6-06f5a9da3608) — classification: No Action Indicated (NAI), source: FDA, date: September 27, 2010
- FDA Inspection 682551 - Neurotron. Inc. - 2010-09-27 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 27, 2010
- FDA Inspection 554398 - Neurotron. Inc. - 2008-12-17 — classification: No Action Indicated (NAI), source: FDA, date: December 17, 2008

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