# Innovative Neurotronics, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/innovative-neurotronics-inc/3a539267-5c38-433f-848a-4f2e6631e5fe

> Inspection records and compliance data for Innovative Neurotronics, Inc. in Reno, Nevada. Access full analysis and detailed observations.

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## Details

- Name: Innovative Neurotronics, Inc.
- FEI Number: 3005694504
- City: Reno
- State: Nevada
- Country Name: United States
- Address Line 1: 4999 Aircenter Cir Ste 103
- Zip Code: 89502

## Related Documents

- [FDA Inspection 1253747 - Innovative Neurotronics, Inc. - 2024-09-26](https://www.keypedia.com/records/fda_inspections/innovative-neurotronics-inc/ca0dbe65-bda9-4c9a-b4ab-e9872b2145a9) — source: FDA, date: September 26, 2024
- [FDA Inspection 1253747 - Innovative Neurotronics, Inc. - 2024-09-26](https://www.keypedia.com/records/fda_inspections/innovative-neurotronics-inc/934e420e-70f4-4cfd-9dcb-a13a2f083cc2) — classification: No Action Indicated (NAI), source: FDA, date: September 26, 2024
- [FDA Inspection 1253747 - Innovative Neurotronics, Inc. - 2024-09-26](https://www.keypedia.com/records/fda_inspections/innovative-neurotronics-inc/f2a78ecd-1abc-4b39-afb3-ace2f7481907) — classification: No Action Indicated (NAI), source: FDA, date: September 26, 2024
- [FDA Inspection 921070 - Innovative Neurotronics, Inc. - 2015-03-25](https://www.keypedia.com/records/fda_inspections/innovative-neurotronics-inc/d83f83aa-f6a7-42d4-8eed-c01fdc8d4f8c) — classification: No Action Indicated (NAI), source: FDA, date: March 25, 2015
- [FDA Inspection 921070 - Innovative Neurotronics, Inc. - 2015-03-25](https://www.keypedia.com/records/fda_inspections/innovative-neurotronics-inc/8dbdcbbe-5043-4bb7-9951-af2686908b8a) — classification: No Action Indicated (NAI), source: FDA, date: March 25, 2015
- [FDA Inspection 676095 - Innovative Neurotronics, Inc. - 2010-07-19](https://www.keypedia.com/records/fda_inspections/innovative-neurotronics-inc/c9e4476f-ec3e-4fe5-879b-69a989e6dbe6) — classification: No Action Indicated (NAI), source: FDA, date: July 19, 2010

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