Warning letter
Cardiomed Supplies, Inc.: warning letter of Sep 21, 2018
FDA warning letter 564967 · Center for Devices and Radiological Health
Key facts
| Reference number | 564967 |
|---|---|
| Company | Cardiomed Supplies, Inc. |
| Subject | CGMP/QSR/Medical Devices/Adulterated |
| Issue date | Sep 21, 2018 |
| Posted date | Oct 30, 2018 |
| Issuing office | Center for Devices and Radiological Health |
| Product type | Devices |
| CFR sections cited | 820 |
| Inspection city | Lindsay |
| Inspection start date | May 28, 2018 |
| Letter on fda.gov | fda.gov |
At a glance
- 1–9 CFR sections cited
- 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: