FDA inspection
Ferrosan Medical Devices Sp. Z o. o.: FDA inspection ending Jan 26, 2023
FDA inspection 1198597 · No Action Indicated (NAI) · Szczecin
Key facts
| Inspection ID | 1198597 |
|---|---|
| Firm | Ferrosan Medical Devices Sp. Z o. o. |
| FEI number | 3007162296 |
| Address | Ul. Koksowa 3 |
| City | Szczecin |
| Country | Poland |
| Fiscal year | 2023 |
| Inspection end date | Jan 26, 2023 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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