Warning letter
G. Dundas Company Inc: warning letter of Dec 13, 2007
FDA warning letter UCM076596 · Seattle District Office
Key facts
| Reference number | UCM076596 |
|---|---|
| Company | G. Dundas Company Inc |
| Subject | CGMP/QSR/Medical Devices/Adulterated/Misbranded |
| Issue date | Dec 13, 2007 |
| Posted date | Dec 13, 2007 |
| Issuing office | Seattle District Office |
| Product type | Devices |
| CFR sections cited | 807.81(a)(3)(i), 820 |
| Country | 3 |
| Inspection city | Black Diamond |
| Inspection ZIP | 98010-9219 |
| Inspection start date | Jun 15, 2007 |
| Letter on fda.gov | web.archive.org |
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: