FDA inspection
Product Quest Manufacturing LLC: FDA inspection ending Jan 27, 2017
FDA inspection 1000036 · Voluntary Action Indicated (VAI) · Daytona Beach, FL
Key facts
| Inspection ID | 1000036 |
|---|---|
| Firm | Product Quest Manufacturing LLC |
| FEI number | 3001554391 |
| Address | 330 Carswell Ave |
| City | Daytona Beach |
| State | FL |
| ZIP | 32117 |
| Country | United States |
| Fiscal year | 2017 |
| Inspection end date | Jan 27, 2017 |
| 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