FDA inspection

Leo Pharma Manufacturing Italy SRL: FDA inspection ending Jul 25, 2019

FDA inspection 1119539 · Voluntary Action Indicated (VAI) · Segrate

Key facts

Inspection ID 1119539
Firm Leo Pharma Manufacturing Italy SRL
FEI number 3002808260
Address Via Ernest Schering 21
City Segrate
Country Italy
Fiscal year 2019
Inspection end date Jul 25, 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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