FDA inspection
Coloplast Hungary Kft: FDA inspection ending Jun 18, 2009
FDA inspection 599050 · Voluntary Action Indicated (VAI) · Tatabanya
Key facts
| Inspection ID | 599050 |
|---|---|
| Firm | Coloplast Hungary Kft |
| FEI number | 3003814961 |
| Address | Buzaviraq ut 15 |
| City | Tatabanya |
| Country | Hungary |
| Fiscal year | 2009 |
| Inspection end date | Jun 18, 2009 |
| 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