FDA inspection
Trident Manufacturing, Inc.: FDA inspection ending Aug 28, 2025
FDA inspection 1279932 · Voluntary Action Indicated (VAI) · Pingree Grove, IL
Key facts
| Inspection ID | 1279932 |
|---|---|
| Firm | Trident Manufacturing, Inc. |
| FEI number | 3008717566 |
| Address | 41w275 Railroad St |
| City | Pingree Grove |
| State | IL |
| ZIP | 60140 |
| Country | United States |
| Fiscal year | 2025 |
| Inspection end date | Aug 28, 2025 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: 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