FDA inspection

Eurofins Amatsi Analytics: FDA inspection ending Feb 4, 2014

FDA inspection 865532 · No Action Indicated (NAI) · Fontenilles

Key facts

Inspection ID 865532
Firm Eurofins Amatsi Analytics
FEI number 3006118993
Address Parc De Genibrat
City Fontenilles
Country France
Fiscal year 2014
Inspection end date Feb 4, 2014
Classification No Action Indicated (NAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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