FDA inspection
Siemens Healthcare Diagnostics Manufacturing Limited: FDA inspection ending Jun 13, 2002
FDA inspection 223001 · No Action Indicated (NAI) · Swords
Key facts
| Inspection ID | 223001 |
|---|---|
| Firm | Siemens Healthcare Diagnostics Manufacturing Limited |
| FEI number | 3007019572 |
| Address | Chapel Lane |
| City | Swords |
| Fiscal year | 2002 |
| Inspection end date | Jun 13, 2002 |
| Classification | No Action Indicated (NAI) |
| 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