FDA inspection
Precision Dose Inc.: FDA inspection ending Jan 28, 2019
FDA inspection 1078690 · Voluntary Action Indicated (VAI) · South Beloit, IL
Key facts
| Inspection ID | 1078690 |
|---|---|
| Firm | Precision Dose Inc. |
| FEI number | 1419861 |
| Address | 722 Progressive Ln |
| City | South Beloit |
| State | IL |
| ZIP | 61080 |
| Country | United States |
| Fiscal year | 2019 |
| Inspection end date | Jan 28, 2019 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- None Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- Yes 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