FDA inspection

AstraZeneca Pharmaceuticals, LP: FDA inspection ending Aug 24, 2017

FDA inspection 1022686 · Voluntary Action Indicated (VAI) · Newark, DE

Key facts

Inspection ID 1022686
Firm AstraZeneca Pharmaceuticals, LP
FEI number 2517100
Address 587 Old Baltimore Pike
City Newark
State DE
ZIP 19702
Country United States
Fiscal year 2017
Inspection end date Aug 24, 2017
Classification Voluntary Action Indicated (VAI)
Project area Foodborne Biological Hazards
Product type Food/Cosmetics

At a glance

  • 1–9 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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