FDA inspection

Astrea Fontaine: FDA inspection ending Dec 11, 2020

FDA inspection 1271540 · Voluntary Action Indicated (VAI) · Fontaine Les Dijon

Key facts

Inspection ID 1271540
Firm Astrea Fontaine
FEI number 3002807473
Address Site De Fontaine, Rue Des Pres Potets
City Fontaine Les Dijon
Country France
Fiscal year 2021
Inspection end date Dec 11, 2020
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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