FDA inspection
Agilent Technologies, Inc.: FDA inspection ending Dec 6, 2019
FDA inspection 1113860 · No Action Indicated (NAI) · Carpinteria, CA
Key facts
| Inspection ID | 1113860 |
|---|---|
| Firm | Agilent Technologies, Inc. |
| FEI number | 2022180 |
| Address | 1170 Mark Ave |
| City | Carpinteria |
| State | CA |
| ZIP | 93013 |
| Country | United States |
| Fiscal year | 2020 |
| Inspection end date | Dec 6, 2019 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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