FDA inspection

Neomend Inc: FDA inspection ending Sep 1, 2015

FDA inspection 941850 · Voluntary Action Indicated (VAI) · Irvine, CA

Key facts

Inspection ID 941850
Firm Neomend Inc
FEI number 3001237235
Address 60 Technology Dr
City Irvine
State CA
ZIP 92618
Country United States
Fiscal year 2015
Inspection end date Sep 1, 2015
Classification Voluntary Action Indicated (VAI)
Project area Bioresearch Monitoring
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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