FDA inspection

LEO Pharma Ireland: FDA inspection ending Jun 3, 2016

FDA inspection 984558 · No Action Indicated (NAI) · Dublin 12

Key facts

Inspection ID 984558
Firm LEO Pharma Ireland
FEI number 3002807468
Address 285 Cashel Road
City Dublin 12
Fiscal year 2016
Inspection end date Jun 3, 2016
Classification No Action Indicated (NAI)
Project area New Drug Evaluation
Product type Drugs

At a glance

  • None Citations
  • None 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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