FDA inspection

AstraZeneca Pharmaceuticals, LP: FDA inspection ending Jun 14, 2006

FDA inspection 432089 · Voluntary Action Indicated (VAI) · Newark, DE

Key facts

Inspection ID 432089
Firm AstraZeneca Pharmaceuticals, LP
FEI number 2517100
Address 587 Old Baltimore Pike
City Newark
State DE
ZIP 19702-1307
Fiscal year 2006
Inspection end date Jun 14, 2006
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
  • 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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