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FDA Inspection
•Neurovision Medical Products Inc•February 13, 2024

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

Record Details

This FDA Inspection record concerns Neurovision Medical Products Inc, with an inspection on February 13, 2024, issued by the Center for Devices and Radiological Health, covering devices.

Company
Neurovision Medical Products Inc
Inspection Date
February 13, 2024
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Sarah A. Hassas (Company Rep)
View Company Profile

ID · 1ceee534-69ed-4478-a1c7-819bfdc76c0b

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1234182
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices

Other FDA inspections of Neurovision Medical Products Inc

3
DateClassificationOfficeProject area
September 30, 2016VAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
November 20, 2012VAICenter for Devices and Radiological HealthCompliance: Devices
September 22, 2010NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Neurovision Medical Products Inc
  • FDA Inspection 986763 - 2016-09-30
  • FDA Inspection 810024 - 2012-11-20
  • FDA Inspection 681607 - 2010-09-22

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