FDA inspection

Amgen, Inc.: FDA inspection ending Oct 3, 2017

FDA inspection 1040847 · No Action Indicated (NAI) · Thousand Oaks, CA

Key facts

Inspection ID 1040847
Firm Amgen, Inc.
FEI number 2026154
Address 1 Amgen Center Dr
City Thousand Oaks
State CA
ZIP 91320-1730
Fiscal year 2018
Inspection end date Oct 3, 2017
Classification No Action Indicated (NAI)
Project area New Drug Evaluation
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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