Warning letter
VIBE Technologies, LLC: warning letter of Apr 11, 2008
FDA warning letter UCM1048345 · Denver District Office
Key facts
| Reference number | UCM1048345 |
|---|---|
| Company | VIBE Technologies, LLC |
| Subject | CGMP/QSR/Medical Devices/Adulterated |
| Issue date | Apr 11, 2008 |
| Posted date | Apr 11, 2008 |
| Issuing office | Denver District Office |
| Product type | Devices |
| CFR sections cited | 807.81(b), 803, 803.17, 820 |
| Country | 3 |
| Inspection city | Greeley |
| Inspection ZIP | 80634-3527 |
| Inspection start date | Nov 5, 2007 |
| 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: