FDA inspection

American Imex: FDA inspection ending Dec 16, 2011

FDA inspection 758825 · Voluntary Action Indicated (VAI) · Irvine, CA

Key facts

Inspection ID 758825
Firm American Imex
FEI number 2083018
Address 16520 Aston
City Irvine
State CA
ZIP 92606
Country United States
Fiscal year 2012
Inspection end date Dec 16, 2011
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: Devices
Product type Devices

At a glance

  • 1–9 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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