Warning letter
Smiths Group Plc.: warning letter of May 24, 2006
FDA warning letter UCM075919 · Center for Devices and Radiological Health
Key facts
| Reference number | UCM075919 |
|---|---|
| Company | Smiths Group Plc. |
| Subject | CGMP for Medical Devices Reporting/Adulterated/Misbranded |
| Issue date | May 24, 2006 |
| Posted date | May 24, 2006 |
| Issuing office | Center for Devices and Radiological Health |
| Product type | Devices |
| CFR sections cited | 803, 803.50(a)(1), 803.50(a)(2), 820 |
| Country | 3 |
| Letter on fda.gov | web.archive.org |
At a glance
- 1–9 CFR sections cited
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: