FDA inspection
Agilent Technologies, Inc.: FDA inspection ending Oct 25, 2018
FDA inspection 1109059 · No Action Indicated (NAI) · Carpinteria, CA
Key facts
| Inspection ID | 1109059 |
|---|---|
| Firm | Agilent Technologies, Inc. |
| FEI number | 2022180 |
| Address | 1170 Mark Ave |
| City | Carpinteria |
| State | CA |
| ZIP | 93013-2918 |
| Fiscal year | 2019 |
| Inspection end date | Oct 25, 2018 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Medical Devices |
| 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
- 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