FDA inspection
Dwyer Precision Products, Inc.: FDA inspection ending Sep 20, 2011
FDA inspection 746726 · Voluntary Action Indicated (VAI) · Jacksonville, FL
Key facts
| Inspection ID | 746726 |
|---|---|
| Firm | Dwyer Precision Products, Inc. |
| FEI number | 1000114410 |
| Address | 266 20th St N |
| City | Jacksonville |
| State | FL |
| ZIP | 32250 |
| Country | United States |
| Fiscal year | 2011 |
| Inspection end date | Sep 20, 2011 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: 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