Warning letter
Beta Biomedical Services, Inc.: warning letter of Apr 19, 2002
FDA warning letter UCM144865 · Dallas District Office
Key facts
| Reference number | UCM144865 |
|---|---|
| Company | Beta Biomedical Services, Inc. |
| Subject | Pulse Oximeter Sensors/Adulterated/Misbranded |
| Issue date | Apr 19, 2002 |
| Posted date | Apr 19, 2002 |
| Issuing office | Dallas District Office |
| Product type | Devices |
| CFR sections cited | 807.3(d), 820.3, 807.81(a)(2) |
| Country | 3 |
| Inspection city | Rowlett |
| Inspection ZIP | 75088-4986 |
| Inspection start date | Dec 6, 2001 |
| Letter on fda.gov | web.archive.org |
At a glance
- 1–9 CFR sections cited
- 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: