FDA inspection
Hemagen Diagnostics Inc: FDA inspection ending May 14, 2026
FDA inspection 1317040 · Voluntary Action Indicated (VAI) · Baltimore, MD
Key facts
| Inspection ID | 1317040 |
|---|---|
| Firm | Hemagen Diagnostics Inc |
| FEI number | 1181055 |
| Address | 2900 Loch Raven Rd |
| City | Baltimore |
| State | MD |
| ZIP | 21218 |
| Country | United States |
| Fiscal year | 2026 |
| Inspection end date | May 14, 2026 |
| 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