FDA inspection

Novartis Manufacturing NV: FDA inspection ending Mar 26, 2014

FDA inspection 874952 · No Action Indicated (NAI) · Puurs-Sint-Amands

Key facts

Inspection ID 874952
Firm Novartis Manufacturing NV
FEI number 3002037047
Address Rijksweg 14
City Puurs-Sint-Amands
Country Belgium
Fiscal year 2014
Inspection end date Mar 26, 2014
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
  • 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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