FDA inspection

Intercos Europe S.p.A: FDA inspection ending Feb 13, 2015

FDA inspection 922885 · Voluntary Action Indicated (VAI) · Agrate Brianza

Key facts

Inspection ID 922885
Firm Intercos Europe S.p.A
FEI number 1000181428
Address Via G. Marconi 84
City Agrate Brianza
Country Italy
Fiscal year 2015
Inspection end date Feb 13, 2015
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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