FDA inspection
Amgen, Inc.: FDA inspection ending May 16, 2017
FDA inspection 1017093 · Voluntary Action Indicated (VAI) · Thousand Oaks, CA
Key facts
| Inspection ID | 1017093 |
|---|---|
| Firm | Amgen, Inc. |
| FEI number | 2026154 |
| Address | 1 Amgen Center Dr |
| City | Thousand Oaks |
| State | CA |
| ZIP | 91320-1730 |
| Fiscal year | 2017 |
| Inspection end date | May 16, 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