FDA inspection

Neurovision Medical Products Inc: FDA inspection ending Sep 22, 2010

FDA inspection 681607 · No Action Indicated (NAI) · Ventura, CA

Key facts

Inspection ID 681607
Firm Neurovision Medical Products Inc
FEI number 1930870
Address 2443 Portola Rd
City Ventura
State CA
ZIP 93003
Country United States
Fiscal year 2010
Inspection end date Sep 22, 2010
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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