FDA inspection

EuroAPI Italy SRL: FDA inspection ending Mar 9, 2018

FDA inspection 1067288 · Voluntary Action Indicated (VAI) · Brindisi

Key facts

Inspection ID 1067288
Firm EuroAPI Italy SRL
FEI number 3003677892
Address Via Angelo Titi 22
City Brindisi
Country Italy
Fiscal year 2018
Inspection end date Mar 9, 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
  • 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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