FDA inspection

AstraZeneca Pharmaceuticals, LP: FDA inspection ending Oct 7, 1999

FDA inspection 5093 · No Action Indicated (NAI) · Newark, DE

Key facts

Inspection ID 5093
Firm AstraZeneca Pharmaceuticals, LP
FEI number 2517100
Address 587 Old Baltimore Pike
City Newark
State DE
ZIP 19702-1307
Fiscal year 2000
Inspection end date Oct 7, 1999
Classification No Action Indicated (NAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • None Citations
  • None 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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