FDA inspection

Neomend Inc: FDA inspection ending Nov 9, 2009

FDA inspection 626365 · No Action Indicated (NAI) · Irvine, CA

Key facts

Inspection ID 626365
Firm Neomend Inc
FEI number 3001237235
Address 60 Technology Dr
City Irvine
State CA
ZIP 92618
Country United States
Fiscal year 2010
Inspection end date Nov 9, 2009
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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