Warning letter
American Medical Devices, Inc.: warning letter of Nov 24, 2003
FDA warning letter UCM147839 · Los Angeles District Office
Key facts
| Reference number | UCM147839 |
|---|---|
| Company | American Medical Devices, Inc. |
| Subject | Quality System Regulation |
| Issue date | Nov 24, 2003 |
| Posted date | Nov 24, 2003 |
| Issuing office | Los Angeles District Office |
| Product type | Devices |
| CFR sections cited | 150, 820 |
| Country | 3 |
| Inspection city | San Bernardino |
| Inspection ZIP | 92401-2021 |
| Inspection start date | Sep 15, 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: