FDA inspection

Pfizer Manufacturing Belgium NV: FDA inspection ending Nov 16, 2017

FDA inspection 1036703 · No Action Indicated (NAI) · Puurs-Sint-Amands

Key facts

Inspection ID 1036703
Firm Pfizer Manufacturing Belgium NV
FEI number 1000654629
Address Rijksweg 12
City Puurs-Sint-Amands
Country Belgium
Fiscal year 2018
Inspection end date Nov 16, 2017
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
  • No Form FDA 483 issued
  • No 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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