Warning letter
Iradimed Corporation: warning letter of Aug 18, 2014
FDA warning letter UCM411895 · Florida District Office
Key facts
| Reference number | UCM411895 |
|---|---|
| Company | Iradimed Corporation |
| Subject | CGMP/QSR/Medical Devices/Adulterated |
| Issue date | Aug 18, 2014 |
| Posted date | Aug 18, 2014 |
| Issuing office | Florida District Office |
| Product type | Devices |
| CFR sections cited | 807.81(a)(3), 820, 807.81(b) |
| Country | 3 |
| Inspection city | orlando |
| Inspection ZIP | 32826 |
| Inspection start date | Apr 7, 2014 |
| Letter on fda.gov | web.archive.org |
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: