FDA inspection

Roquette Freres: FDA inspection ending Feb 10, 2017

FDA inspection 1010367 · Voluntary Action Indicated (VAI) · Lestrem

Key facts

Inspection ID 1010367
Firm Roquette Freres
FEI number 1000114558
Address 1 rue de la Haute Loge
City Lestrem
Country France
Fiscal year 2017
Inspection end date Feb 10, 2017
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type Drugs

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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