FDA inspection
Agilent Technologies, Inc.: FDA inspection ending Jul 6, 2015
FDA inspection 936087 · Voluntary Action Indicated (VAI) · Santa Clara, CA
Key facts
| Inspection ID | 936087 |
|---|---|
| Firm | Agilent Technologies, Inc. |
| FEI number | 2916205 |
| Address | 5301 Stevens Creek Blvd |
| City | Santa Clara |
| State | CA |
| ZIP | 95051 |
| Country | United States |
| Fiscal year | 2015 |
| Inspection end date | Jul 6, 2015 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 1–9 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