FDA inspection
AGILENT TECHNOLOGIES INC./US: FDA inspection ending Aug 27, 2020
FDA inspection 1130381 · No Action Indicated (NAI) · Frederick, CO
Key facts
| Inspection ID | 1130381 |
|---|---|
| Firm | AGILENT TECHNOLOGIES INC./US |
| FEI number | 3014531850 |
| Address | Agilent Technologies, Inc., 7051 Eagle Blvd |
| City | Frederick |
| State | CO |
| ZIP | 80504-5875 |
| Fiscal year | 2020 |
| Inspection end date | Aug 27, 2020 |
| Classification | No Action Indicated (NAI) |
| Project area | New Drug Evaluation |
| Product type | Drugs |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- Yes 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