FDA inspection
Terumo Cardiovascular Systems Corporation: FDA inspection ending Feb 11, 2009
FDA inspection 561886 · No Action Indicated (NAI) · Elkton, MD
Key facts
| Inspection ID | 561886 |
|---|---|
| Firm | Terumo Cardiovascular Systems Corporation |
| FEI number | 3000204839 |
| Address | 125 Blue Ball Rd |
| City | Elkton |
| State | MD |
| ZIP | 21921 |
| Country | United States |
| Fiscal year | 2009 |
| Inspection end date | Feb 11, 2009 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 10–99 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