Warning letter
Technomed Europe: warning letter of Sep 17, 2008
FDA warning letter UCM1048132 · Center for Devices and Radiological Health
Key facts
| Reference number | UCM1048132 |
|---|---|
| Company | Technomed Europe |
| Subject | CGMP/QSR/Medical Devices/Adulterated |
| Issue date | Sep 17, 2008 |
| Posted date | Sep 17, 2008 |
| Issuing office | Center for Devices and Radiological Health |
| Product type | Devices |
| CFR sections cited | 820 |
| Country | 3 |
| Inspection city | Maastricht-Airport |
| Inspection start date | Jun 9, 2008 |
| 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: