FDA inspection
Aurora Products, Inc.: FDA inspection ending Jan 28, 2010
FDA inspection 643172 · Voluntary Action Indicated (VAI) · Orange, CT
Key facts
| Inspection ID | 643172 |
|---|---|
| Firm | Aurora Products, Inc. |
| FEI number | 3002286594 |
| Address | 205 Edison Rd |
| City | Orange |
| State | CT |
| ZIP | 06477 |
| Country | United States |
| Fiscal year | 2010 |
| Inspection end date | Jan 28, 2010 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Foodborne Biological Hazards |
| Product type | Food/Cosmetics |
At a glance
- None Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No 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