FDA inspection

EUROAPI FRANCE: FDA inspection ending Sep 16, 2016

FDA inspection 987999 · Voluntary Action Indicated (VAI) · Vertolaye

Key facts

Inspection ID 987999
Firm EUROAPI FRANCE
FEI number 1463
Address Rue Du Bourg
City Vertolaye
Country France
Fiscal year 2016
Inspection end date Sep 16, 2016
Classification Voluntary Action Indicated (VAI)
Project area Monitoring of Marketed Animal Drugs, Feed, and Devices
Product type Veterinary

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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