Warning letter
Northwest Medical Physics Equipment, Inc.: warning letter of Dec 21, 2007
FDA warning letter UCM076604 · Seattle District Office
Key facts
| Reference number | UCM076604 |
|---|---|
| Company | Northwest Medical Physics Equipment, Inc. |
| Subject | CGMP/QSR/Manufacture/Packing/Storage/Installation/Adulterated |
| Issue date | Dec 21, 2007 |
| Posted date | Dec 21, 2007 |
| Issuing office | Seattle District Office |
| Product type | Devices |
| CFR sections cited | 806.10(b), 803, 803.17, 806, 803.17(a)(1), 803.50(a)(2), 820, 806.10(a)(2) |
| Country | 3 |
| Inspection city | Kalona |
| Inspection ZIP | 52247-9589 |
| Inspection start date | Jun 20, 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: