Warning letter
Meridian Bioscience, Inc: warning letter of Dec 22, 2025
FDA warning letter 720826 · Center for Devices and Radiological Health
Key facts
| Reference number | 720826 |
|---|---|
| Company | Meridian Bioscience, Inc |
| Subject | CGMP/QSR/Medical Devices/Adulterated |
| Issue date | Dec 22, 2025 |
| Posted date | Jan 27, 2026 |
| Issuing office | Center for Devices and Radiological Health |
| Product type | Devices |
| CFR sections cited | 803, 820, 806, 806.10, 803.50(a)(2), 803.3 |
| Inspection city | North Billerica |
| Inspection ZIP | 01862 |
| Inspection start date | Aug 5, 2025 |
| Letter on fda.gov | fda.gov |
At a glance
- 1–9 CFR sections cited
- OAI Linked inspection classification
- Yes Form FDA 483 issued
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA warning letters
FDA warning letters notify a firm of significant regulatory violations found during an inspection or review and request prompt corrective action.
Source: U.S. Food and Drug Administration (FDA), Warning Letters · Source date: