FDA inspection
Philips Medical Systems Technologies Ltd: FDA inspection ending Jan 12, 2023
FDA inspection 1195326 · Voluntary Action Indicated (VAI) · Haifa
Key facts
| Inspection ID | 1195326 |
|---|---|
| Firm | Philips Medical Systems Technologies Ltd |
| FEI number | 3008581796 |
| Address | Building 34, Advanced Technology Center Matam |
| City | Haifa |
| Country | Israel |
| Fiscal year | 2023 |
| Inspection end date | Jan 12, 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