Warning letter
GUANGDONG BIOLIGHT MEDITECH CO., LTD: warning letter of Jan 2, 2013
FDA warning letter 381918 · Center for Devices and Radiological Health
Key facts
| Reference number | 381918 |
|---|---|
| Company | GUANGDONG BIOLIGHT MEDITECH CO., LTD |
| Subject | CGMP for Medical Devices/QSR/Medical Device Reporting/Adulterated/Misbranded |
| Issue date | Jan 2, 2013 |
| Posted date | Jan 2, 2013 |
| Issuing office | Center for Devices and Radiological Health |
| Product type | Devices |
| CFR sections cited | 803.50(b), 801.1, 803, 803.3, 803.17, 803.50, 803.53, 820 |
| Inspection city | Zhuhai |
| Inspection start date | Aug 20, 2012 |
| Letter on fda.gov | web.archive.org |
At a glance
- 1–9 CFR sections cited
- ADC 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: