FDA inspection

Randox Laboratories, Limited: FDA inspection ending Jun 29, 2006

FDA inspection 434871 · Voluntary Action Indicated (VAI) · Crumlin

Key facts

Inspection ID 434871
Firm Randox Laboratories, Limited
FEI number 3004493545
Address 44 Largy Road
City Crumlin
Fiscal year 2006
Inspection end date Jun 29, 2006
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Med Devices
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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