FDA inspection

Laboratoire Icare: FDA inspection ending Mar 18, 2014

FDA inspection 875089 · No Action Indicated (NAI) · Saint-Beauzire

Key facts

Inspection ID 875089
Firm Laboratoire Icare
FEI number 3008220949
Address Biopole, Clermont Limagne
City Saint-Beauzire
Country France
Fiscal year 2014
Inspection end date Mar 18, 2014
Classification No Action Indicated (NAI)
Project area Drug Quality Assurance
Product type Drugs

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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