FDA inspection
Palodex Group Oy: FDA inspection ending Aug 16, 2019
FDA inspection 1156767 · Tuusula
Key facts
| Inspection ID | 1156767 |
|---|---|
| Firm | Palodex Group Oy |
| FEI number | 3005383085 |
| Address | Nahkelantie 160 |
| City | Tuusula |
| Fiscal year | 2019 |
| Inspection end date | Aug 16, 2019 |
| Project area | Compliance: Medical Devices |
| Product type | Devices |
At a glance
- None 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