FDA inspection
Frontida Biopharm, LLC: FDA inspection ending Oct 24, 2025
FDA inspection 1283762 · Voluntary Action Indicated (VAI) · Aurora, IL
Key facts
| Inspection ID | 1283762 |
|---|---|
| Firm | Frontida Biopharm, LLC |
| FEI number | 3008087151 |
| Address | 2500 Molitor Rd |
| City | Aurora |
| State | IL |
| ZIP | 60502 |
| Country | United States |
| Fiscal year | 2026 |
| Inspection end date | Oct 24, 2025 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
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