Warning letter
Vitang Technology LLC: warning letter of Jun 12, 2023
FDA warning letter 653455 · Center for Devices and Radiological Health
Key facts
| Reference number | 653455 |
|---|---|
| Company | Vitang Technology LLC |
| Subject | CGMP/QSR/Medical Devices/Adulterated |
| Issue date | Jun 12, 2023 |
| Posted date | Jun 20, 2023 |
| Issuing office | Center for Devices and Radiological Health |
| Product type | Devices |
| CFR sections cited | 807.81(b), 807.97, 807.81(a)(3), 820 |
| Inspection city | Tustin |
| Inspection ZIP | 92780-7224 |
| Inspection start date | Jan 24, 2023 |
| Letter on fda.gov | fda.gov |
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: