FDA inspection

Intercos Europe SpA: FDA inspection ending Nov 29, 2024

FDA inspection 1256045 · Voluntary Action Indicated (VAI) · Dovera

Key facts

Inspection ID 1256045
Firm Intercos Europe SpA
FEI number 3005291719
Address Strada Provinciale Bergamina 472 Km. 21,150
City Dovera
Country Italy
Fiscal year 2025
Inspection end date Nov 29, 2024
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • 1–9 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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