FDA inspection
Haemotec, a division of Fresenius Medical Care Canada Inc.: FDA inspection ending Sep 13, 2012
FDA inspection 802502 · Voluntary Action Indicated (VAI) · Vaudreuil-Dorion
Key facts
| Inspection ID | 802502 |
|---|---|
| Firm | Haemotec, a division of Fresenius Medical Care Canada Inc. |
| FEI number | 3005578748 |
| Address | 383 Joseph-Carrier St |
| City | Vaudreuil-Dorion |
| Country | Canada |
| Fiscal year | 2012 |
| Inspection end date | Sep 13, 2012 |
| Classification | Voluntary Action Indicated (VAI) |
| 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