FDA inspection
Elos Medtech Timmersdala AB: FDA inspection ending Oct 14, 2010
FDA inspection 698517 · Official Action Indicated (OAI) · Timmersdala
Key facts
| Inspection ID | 698517 |
|---|---|
| Firm | Elos Medtech Timmersdala AB |
| FEI number | 3003847101 |
| Address | Backedalsvagen 5/ P.O. Box 45 |
| City | Timmersdala |
| Country | Sweden |
| Fiscal year | 2011 |
| Inspection end date | Oct 14, 2010 |
| Classification | Official Action Indicated (OAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- 1–9 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