FDA inspection
Agilent Technologies Denmark ApS: FDA inspection ending Nov 27, 2003
FDA inspection 309501 · Glostrup
Key facts
| Inspection ID | 309501 |
|---|---|
| Firm | Agilent Technologies Denmark ApS |
| FEI number | 3002806778 |
| Address | 42 PRODUKTIONSVEJ |
| City | Glostrup |
| Fiscal year | 2004 |
| Inspection end date | Nov 27, 2003 |
| Project area | Compliance: Med 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
- 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