FDA inspection
Agilent Technologies Denmark ApS: FDA inspection ending Jan 15, 2015
FDA inspection 914699 · No Action Indicated (NAI) · Glostrup
Key facts
| Inspection ID | 914699 |
|---|---|
| Firm | Agilent Technologies Denmark ApS |
| FEI number | 3002806778 |
| Address | Produktionsvej 42 |
| City | Glostrup |
| Country | Denmark |
| Fiscal year | 2015 |
| Inspection end date | Jan 15, 2015 |
| 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
- 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