Warning letter
Rite-Dent Manufacturing Corp.: warning letter of Dec 2, 2005
FDA warning letter UCM075724 · Florida District Office
Key facts
| Reference number | UCM075724 |
|---|---|
| Company | Rite-Dent Manufacturing Corp. |
| Subject | Medical Device Reporting Regulations/Quality System Regulation/Adulterated/Misbranded |
| Issue date | Dec 2, 2005 |
| Posted date | Dec 2, 2005 |
| Issuing office | Florida District Office |
| Product type | Devices |
| CFR sections cited | 803.17, 803, 820.40, 820 |
| Country | 3 |
| Inspection city | Hialeah |
| Inspection ZIP | 33013-2920 |
| Inspection start date | Sep 9, 2005 |
| 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: