FDA inspection

Neurovision Medical Products Inc: FDA inspection ending Oct 3, 2019

FDA inspection 1135497 · Voluntary Action Indicated (VAI) · Ventura, CA

Key facts

Inspection ID 1135497
Firm Neurovision Medical Products Inc
FEI number 1930870
Address 2443 Portola Rd
City Ventura
State CA
ZIP 93003-7726
Fiscal year 2020
Inspection end date Oct 3, 2019
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Medical Devices
Product type Devices

At a glance

  • None Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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