FDA inspection
Palodex Group Oy: FDA inspection ending Sep 5, 2012
FDA inspection 800785 · Voluntary Action Indicated (VAI) · Tuusula
Key facts
| Inspection ID | 800785 |
|---|---|
| Firm | Palodex Group Oy |
| FEI number | 3005383085 |
| Address | Nahkelantie 160 |
| City | Tuusula |
| Country | Finland |
| Fiscal year | 2012 |
| Inspection end date | Sep 5, 2012 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: 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