Warning letter
American Sunlight, Inc.: warning letter of Mar 12, 2003
FDA warning letter UCM147361 · Los Angeles District Office
Key facts
| Reference number | UCM147361 |
|---|---|
| Company | American Sunlight, Inc. |
| Subject | GMP Requirements for the Quality System Regulation/Adulterated |
| Issue date | Mar 12, 2003 |
| Posted date | Mar 12, 2003 |
| Issuing office | Los Angeles District Office |
| Product type | Devices |
| CFR sections cited | 820.5, 820.40, 820 |
| Country | 3 |
| Inspection city | Huntington Beach |
| Inspection ZIP | 92647-3500 |
| Inspection start date | Jan 16, 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: