Warning letter
Defibtech, LLC [ARCHIVED]: warning letter of Sep 22, 2010
FDA warning letter 133290 · New England District Office
Key facts
| Reference number | 133290 |
|---|---|
| Company | Defibtech, LLC [ARCHIVED] |
| Subject | CGMP/QSR/Medical Devices/Adulterated |
| Issue date | Sep 22, 2010 |
| Posted date | Sep 22, 2010 |
| Issuing office | New England District Office |
| Product type | Devices |
| CFR sections cited | 806.10(a)(1), 820 |
| Inspection city | Guilford |
| Inspection ZIP | 06437 |
| Inspection start date | Jul 29, 2010 |
| 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: