FDA inspection
BONALIVE LTD: FDA inspection ending Dec 17, 2014
FDA inspection 909027 · Voluntary Action Indicated (VAI) · Turku Varsinais-Suomi
Key facts
| Inspection ID | 909027 |
|---|---|
| Firm | BONALIVE LTD |
| FEI number | 3008328709 |
| Address | Biolinja 12 |
| City | Turku Varsinais-Suomi |
| Country | Finland |
| Fiscal year | 2015 |
| Inspection end date | Dec 17, 2014 |
| 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