FDA inspection
Intermex Products USA, Ltd: FDA inspection ending Nov 2, 2007
FDA inspection 496014 · Voluntary Action Indicated (VAI) · Grand Prairie, TX
Key facts
| Inspection ID | 496014 |
|---|---|
| Firm | Intermex Products USA, Ltd |
| FEI number | 1640978 |
| Address | 1375 Avenue S Ste 300 |
| City | Grand Prairie |
| State | TX |
| ZIP | 75050-1293 |
| Fiscal year | 2008 |
| Inspection end date | Nov 2, 2007 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Foodborne Biological Hazard |
| Product type | Food/Cosmetics |
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
- 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