# Neurovision Medical Products Inc - Inspection Records

Source: https://www.keypedia.com/companies/neurovision-medical-products-inc/65b51d9f-3c9c-43f0-9d1f-69503d2eaaf5

> Inspection records and compliance data for Neurovision Medical Products Inc in Ventura, California. Access full analysis and detailed observations.

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## Details

- Name: Neurovision Medical Products Inc
- FEI Number: 1930870
- City: Ventura
- State: California
- Country Name: United States
- Address Line 1: 353 San Jon Rd
- Zip Code: 93001

## Related Documents

- [FDA Inspection 1234182 - Neurovision Medical Products Inc - 2024-02-13](https://www.keypedia.com/records/fda_inspections/neurovision-medical-products-inc/0066107c-0ed1-4584-bc0d-244efd3768b4) — classification: No Action Indicated (NAI), source: FDA, date: February 13, 2024
- [FDA Inspection 1234182 - Neurovision Medical Products Inc - 2024-02-13](https://www.keypedia.com/records/fda_inspections/neurovision-medical-products-inc/1ceee534-69ed-4478-a1c7-819bfdc76c0b) — classification: No Action Indicated (NAI), source: FDA, date: February 13, 2024
- [FDA Inspection 986763 - Neurovision Medical Products Inc - 2016-09-30](https://www.keypedia.com/records/fda_inspections/neurovision-medical-products-inc/362fb05f-01ca-4744-97d8-05d4a1a94101) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 30, 2016
- [FDA Inspection 986763 - Neurovision Medical Products Inc - 2016-09-30](https://www.keypedia.com/records/fda_inspections/neurovision-medical-products-inc/691cf43e-5685-4653-b85b-cd8496bd1814) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 30, 2016
- [FDA Inspection 810024 - Neurovision Medical Products Inc - 2012-11-20](https://www.keypedia.com/records/fda_inspections/neurovision-medical-products-inc/67ebc317-af83-4c35-abc5-ed3a61793d55) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 20, 2012
- [FDA Inspection 681607 - Neurovision Medical Products Inc - 2010-09-22](https://www.keypedia.com/records/fda_inspections/neurovision-medical-products-inc/7a2df0b8-597f-40ef-9129-a054e03449a0) — classification: No Action Indicated (NAI), source: FDA, date: September 22, 2010

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