FDA inspection

Fareva Amboise: FDA inspection ending Dec 13, 2018

FDA inspection 1100819 · Voluntary Action Indicated (VAI) · Poce Sur Cisse

Key facts

Inspection ID 1100819
Firm Fareva Amboise
FEI number 3000234005
Address Zone Industrielle, 29 route des Industries
City Poce Sur Cisse
Country France
Fiscal year 2019
Inspection end date Dec 13, 2018
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
  • 10–99 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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