FDA inspection
Agilent Technologies, Inc.: FDA inspection ending Dec 15, 2004
FDA inspection 359806 · Santa Clara, CA
Key facts
| Inspection ID | 359806 |
|---|---|
| Firm | Agilent Technologies, Inc. |
| FEI number | 2916205 |
| Address | 5301 Stevens Creek Blvd |
| City | Santa Clara |
| State | CA |
| ZIP | 95051-7201 |
| Fiscal year | 2005 |
| Inspection end date | Dec 15, 2004 |
| Project area | Rad Cntrl & Hlth Safety Act (RCHSA) Auth |
| Product type | Devices |
At a glance
- None Citations
- None 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