Warning letter
Trimed Inc: warning letter of Jun 30, 2016
FDA warning letter 494255 · Los Angeles District Office
Key facts
| Reference number | 494255 |
|---|---|
| Company | Trimed Inc |
| Subject | CGMP/QSR/Medical Devices/Adulterated |
| Issue date | Jun 30, 2016 |
| Posted date | Aug 2, 2016 |
| Issuing office | Los Angeles District Office |
| Product type | Devices |
| CFR sections cited | 803.3, 803.17, 806.10, 803.50(a)(1), 803.50(a)(2), 820, 803.50(a) |
| Inspection city | Valencia |
| Inspection ZIP | 91355 |
| Inspection start date | Mar 7, 2016 |
| 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: