FDA inspection

Charles River Laboratories France - CRLF SAS: FDA inspection ending Apr 25, 2019

FDA inspection 1087366 · Voluntary Action Indicated (VAI) · Ecully

Key facts

Inspection ID 1087366
Firm Charles River Laboratories France - CRLF SAS
FEI number 3005503876
Address 9 Allee Moulin Berger
City Ecully
Fiscal year 2019
Inspection end date Apr 25, 2019
Classification Voluntary Action Indicated (VAI)
Project area New Drug Evaluation
Product type Drugs

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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