FDA inspection

AstraZeneca Pharmaceuticals LP: FDA inspection ending Nov 10, 2010

FDA inspection 696033 · Voluntary Action Indicated (VAI) · Wilmington, DE

Key facts

Inspection ID 696033
Firm AstraZeneca Pharmaceuticals LP
FEI number 2518137
Address 1800 Concord Pike
City Wilmington
State DE
ZIP 19897
Country United States
Fiscal year 2011
Inspection end date Nov 10, 2010
Classification Voluntary Action Indicated (VAI)
Project area Bioresearch Monitoring
Product type Drugs

At a glance

  • None Citations
  • 1–9 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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