Warning letter
Trilliant Surgical, LTD [ARCHIVED]: warning letter of May 3, 2010
FDA warning letter 108307 · Dallas District Office
Key facts
| Reference number | 108307 |
|---|---|
| Company | Trilliant Surgical, LTD [ARCHIVED] |
| Subject | CGMP/QSR/Medical Devices/Adulterated/Misbranded |
| Issue date | May 3, 2010 |
| Posted date | May 3, 2010 |
| Issuing office | Dallas District Office |
| Product type | Devices |
| CFR sections cited | 806.1, 806.2(i), 820, 806.10(a)(1), 803, 806 |
| Inspection city | Houston |
| Inspection ZIP | 77007 |
| Inspection start date | Nov 30, 2009 |
| 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: