FDA inspection
Teleflex Medical, Inc.: FDA inspection ending Oct 24, 2012
FDA inspection 806348 · No Action Indicated (NAI) · Mansfield, MA
Key facts
| Inspection ID | 806348 |
|---|---|
| Firm | Teleflex Medical, Inc. |
| FEI number | 1221601 |
| Address | 375 Forbes Blvd |
| City | Mansfield |
| State | MA |
| ZIP | 02048 |
| Country | United States |
| Fiscal year | 2013 |
| Inspection end date | Oct 24, 2012 |
| 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
- 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