FDA inspection
Proven Process Medical Devices, Inc.: FDA inspection ending Dec 20, 2006
FDA inspection 455717 · No Action Indicated (NAI) · Mansfield, MA
Key facts
| Inspection ID | 455717 |
|---|---|
| Firm | Proven Process Medical Devices, Inc. |
| FEI number | 3003174284 |
| Address | 110 Forbes Blvd |
| City | Mansfield |
| State | MA |
| ZIP | 02048-1145 |
| Fiscal year | 2007 |
| Inspection end date | Dec 20, 2006 |
| Classification | No Action Indicated (NAI) |
| Project area | Product Evaluation: 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
- 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