FDA inspection

AstraZeneca AB: FDA inspection ending Dec 1, 2022

FDA inspection 1248349 · Voluntary Action Indicated (VAI) · Sodertalje

Key facts

Inspection ID 1248349
Firm AstraZeneca AB
FEI number 3002806411
Address Forskargatan 18 Se-151 36 Se-151 36
City Sodertalje
Country Sweden
Fiscal year 2023
Inspection end date Dec 1, 2022
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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