Warning letter
U.O. Equipment Company: warning letter of Jun 11, 2003
FDA warning letter UCM147537 · Dallas District Office
Key facts
| Reference number | UCM147537 |
|---|---|
| Company | U.O. Equipment Company |
| Subject | Quality System Regulation/Good Manufacuring Practice/Medical Devices/Adulterated |
| Issue date | Jun 11, 2003 |
| Posted date | Jun 11, 2003 |
| Issuing office | Dallas District Office |
| Product type | Devices |
| CFR sections cited | 803.17, 803.17(a)(1), 803.17(a)(2), 820, 807.20(a), 807.21(b) |
| Country | 3 |
| Inspection city | Houston |
| Inspection ZIP | 77092-6401 |
| Inspection start date | Feb 11, 2003 |
| 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: