Warning letter
Body Vibes: warning letter of Apr 3, 2000
FDA warning letter UCM068298 · Baltimore District Office
Key facts
| Reference number | UCM068298 |
|---|---|
| Company | Body Vibes |
| Subject | Body Vibes System I & II |
| Issue date | Apr 3, 2000 |
| Posted date | Apr 3, 2000 |
| Issuing office | Baltimore District Office |
| Product type | Devices |
| Country | 3 |
| Inspection city | Louisa |
| Inspection ZIP | 23093-4307 |
| Inspection start date | Nov 10, 1999 |
| Letter on fda.gov | web.archive.org |
At a glance
- 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: