FDA inspection

AstraZeneca Pharmaceuticals LP: FDA inspection ending Jan 27, 2017

FDA inspection 1001245 · Voluntary Action Indicated (VAI) · Frederick, MD

Key facts

Inspection ID 1001245
Firm AstraZeneca Pharmaceuticals LP
FEI number 3002617771
Address 633 Research Dr
City Frederick
State MD
ZIP 21703-8619
Fiscal year 2017
Inspection end date Jan 27, 2017
Classification Voluntary Action Indicated (VAI)
Project area New Drug Evaluation
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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