# Neurovision Medical Products Inc – FDA Inspection, Feb 13, 2024

Source: https://www.keypedia.com/records/fda_inspections/neurovision-medical-products-inc/1ceee534-69ed-4478-a1c7-819bfdc76c0b
Source feed: FDA_Inspections

> FDA inspection 1234182 of Neurovision Medical Products Inc, February 13, 2024. Classification: No Action Indicated (NAI). 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1234182
- Company Name: Neurovision Medical Products Inc
- Inspection Date: 2024-02-13
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 986763 - 2016-09-30](https://www.keypedia.com/records/fda_inspections/neurovision-medical-products-inc/691cf43e-5685-4653-b85b-cd8496bd1814)
- [FDA Inspection 810024 - 2012-11-20](https://www.keypedia.com/records/fda_inspections/neurovision-medical-products-inc/67ebc317-af83-4c35-abc5-ed3a61793d55)
- FDA Inspection 681607 - 2010-09-22

## Related Officers

- [Company Rep](https://www.keypedia.com/people/sarah-a-hassas/4f142d54-fc28-4bd5-82ad-7e6fa443688c)

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

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7