FDA inspection

Patheon Italia S.p.A.: FDA inspection ending May 20, 2016

FDA inspection 977718 · Voluntary Action Indicated (VAI) · Monza

Key facts

Inspection ID 977718
Firm Patheon Italia S.p.A.
FEI number 3003065803
Address Viale Gian Battista Stucchi 110
City Monza
Country Italy
Fiscal year 2016
Inspection end date May 20, 2016
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
  • Yes Establishment inspection report (EIR) exists
  • 10–99 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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