FDA inspection

Lundbeck Pharmaceuticals Italy S.p.A.: FDA inspection ending Mar 13, 2009

FDA inspection 575028 · No Action Indicated (NAI) · Padova

Key facts

Inspection ID 575028
Firm Lundbeck Pharmaceuticals Italy S.p.A.
FEI number 3002808449
Address Zona Industriale Quarta Strada 2
City Padova
Country Italy
Fiscal year 2009
Inspection end date Mar 13, 2009
Classification No Action Indicated (NAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • Yes 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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