FDA inspection

Eurofins Biolab Srl: FDA inspection ending Mar 15, 2019

FDA inspection 1119905 · Voluntary Action Indicated (VAI) · Poggibonsi

Key facts

Inspection ID 1119905
Firm Eurofins Biolab Srl
FEI number 3010492524
Address Via Reno 2
City Poggibonsi
Country Italy
Fiscal year 2019
Inspection end date Mar 15, 2019
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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