FDA inspection
Hatch Product Development LLC: FDA inspection ending Dec 11, 2025
FDA inspection 1295192 · Voluntary Action Indicated (VAI) · Waukegan, IL
Key facts
| Inspection ID | 1295192 |
|---|---|
| Firm | Hatch Product Development LLC |
| FEI number | 3030438338 |
| Address | 2330 Ernie Krueger Cir |
| City | Waukegan |
| State | IL |
| ZIP | 60087 |
| Country | United States |
| Fiscal year | 2026 |
| Inspection end date | Dec 11, 2025 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: 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