FDA inspection
Philips Medizin Systeme Boeblingen Gmbh: FDA inspection ending Nov 18, 2004
FDA inspection 355662 · Official Action Indicated (OAI) · Boblingen
Key facts
| Inspection ID | 355662 |
|---|---|
| Firm | Philips Medizin Systeme Boeblingen Gmbh |
| FEI number | 3002807167 |
| Address | Hewlett-Packard-Str. 2 |
| City | Boblingen |
| Fiscal year | 2005 |
| Inspection end date | Nov 18, 2004 |
| Classification | Official Action Indicated (OAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
| Warning letter | UCM075400 |
At a glance
- None Citations
- 1–9 Posted citations
- Yes 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