FDA inspection

DIO USA: FDA inspection ending Nov 16, 2009

FDA inspection 627607 · Voluntary Action Indicated (VAI) · Los Angeles, CA

Key facts

Inspection ID 627607
Firm DIO USA
FEI number 3006400105
Address 3540 Wilshire Blvd Ste 1104
City Los Angeles
State CA
ZIP 90010
Country United States
Fiscal year 2010
Inspection end date Nov 16, 2009
Classification Voluntary Action Indicated (VAI)
Project area Compliance: 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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