FDA inspection
Philips Medical Systems DMC GmbH: FDA inspection ending Jan 19, 2023
FDA inspection 1195414 · Voluntary Action Indicated (VAI) · Hamburg
Key facts
| Inspection ID | 1195414 |
|---|---|
| Firm | Philips Medical Systems DMC GmbH |
| FEI number | 3003768251 |
| Address | Development And Manufacturing Ctr., Rontgenstr. 24-26 |
| City | Hamburg |
| Country | Germany |
| Fiscal year | 2023 |
| Inspection end date | Jan 19, 2023 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- 1–9 Citations
- 1–9 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