Warning letter
Rex Implants Inc.: warning letter of Mar 12, 2025
FDA warning letter 676429 · Center for Devices and Radiological Health
Key facts
| Reference number | 676429 |
|---|---|
| Company | Rex Implants Inc. |
| Subject | Investigational Device Exemptions (IDE)/Premarket Approval Application (PMA) Adulterated Device |
| Issue date | Mar 12, 2025 |
| Posted date | Mar 25, 2025 |
| Issuing office | Center for Devices and Radiological Health |
| Product type | Devices |
| CFR sections cited | 807.81(b) |
| Inspection city | Columbus |
| Inspection ZIP | 43215 |
| Inspection start date | Dec 5, 2023 |
| 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: