FDA inspection
Intermex Products USA, Ltd: FDA inspection ending Mar 11, 2026
FDA inspection 1310136 · No Action Indicated (NAI) · Grand Prairie, TX
Key facts
| Inspection ID | 1310136 |
|---|---|
| Firm | Intermex Products USA, Ltd |
| FEI number | 1640978 |
| Address | 1375 Avenue S Ste 300 |
| City | Grand Prairie |
| State | TX |
| ZIP | 75050 |
| Country | United States |
| Fiscal year | 2026 |
| Inspection end date | Mar 11, 2026 |
| Classification | No Action Indicated (NAI) |
| Project area | Foodborne Biological Hazards |
| Product type | Food/Cosmetics |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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