FDA inspection
Medical Device Consulting: FDA inspection ending Sep 29, 2005
FDA inspection 397775 · Voluntary Action Indicated (VAI) · Centerville, MA
Key facts
| Inspection ID | 397775 |
|---|---|
| Firm | Medical Device Consulting |
| FEI number | 3003160325 |
| Address | 344 Annable Point Rd |
| City | Centerville |
| State | MA |
| ZIP | 02632-2402 |
| Fiscal year | 2005 |
| Inspection end date | Sep 29, 2005 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Product Evaluation: Med 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