FDA inspection
Sorin CRM USA, INC: FDA inspection ending Feb 23, 2000
FDA inspection 14571 · No Action Indicated (NAI) · Plymouth, MN
Key facts
| Inspection ID | 14571 |
|---|---|
| Firm | Sorin CRM USA, INC |
| FEI number | 2182863 |
| Address | 2905 Northwest Blvd Ste 40 |
| City | Plymouth |
| State | MN |
| ZIP | 55441-2673 |
| Fiscal year | 2000 |
| Inspection end date | Feb 23, 2000 |
| Classification | No Action Indicated (NAI) |
| Project area | Postmarket Assurance: Med Devices |
| Product type | Devices |
At a glance
- None Citations
- None 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