FDA inspection
Product Quest Manufacturing LLC: FDA inspection ending Nov 6, 2015
FDA inspection 948191 · Voluntary Action Indicated (VAI) · Daytona Beach, FL
Key facts
| Inspection ID | 948191 |
|---|---|
| Firm | Product Quest Manufacturing LLC |
| FEI number | 3001554391 |
| Address | 330 Carswell Ave |
| City | Daytona Beach |
| State | FL |
| ZIP | 32117 |
| Country | United States |
| Fiscal year | 2016 |
| Inspection end date | Nov 6, 2015 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None 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