Warning letter
Orthoton BV: warning letter of Jun 29, 2004
FDA warning letter UCM146862 · Center for Devices and Radiological Health
Key facts
| Reference number | UCM146862 |
|---|---|
| Company | Orthoton BV |
| Subject | GMP Requirements for Quality System Regulation/Dental Products/Adulterated |
| Issue date | Jun 29, 2004 |
| Posted date | Jun 29, 2004 |
| Issuing office | Center for Devices and Radiological Health |
| Product type | Devices |
| CFR sections cited | 803, 803.17(a)(1), 820.40 |
| Country | 3 |
| Inspection city | Gorinchem |
| Inspection start date | Mar 1, 2004 |
| 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: