FDA Inspection 1234182 — Neurovision Medical Products Inc

Neurovision Medical Products Inc — FEI 1930870

The FDA completed an inspection of Neurovision Medical Products Inc on Feb 13, 2024 in Ventura, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Feb 13, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Ventura, CA (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.