Warning letter
G&B; Electronic Designs Limited: warning letter of Apr 24, 2007
FDA warning letter UCM076364 · Center for Devices and Radiological Health
Key facts
| Reference number | UCM076364 |
|---|---|
| Company | G&B; Electronic Designs Limited |
| Subject | CGMP/QSR/Medical Devices/Adulterated/Misbranded |
| Issue date | Apr 24, 2007 |
| Posted date | Apr 24, 2007 |
| Issuing office | Center for Devices and Radiological Health |
| Product type | Devices |
| CFR sections cited | 820, 806, 806.10, 807, 807.40(a) |
| Country | 3 |
| Inspection city | Bordon |
| Inspection start date | Nov 20, 2006 |
| Letter on fda.gov | web.archive.org |
At a glance
- 1–9 CFR sections cited
- NAI 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: