Warning letter
C & E GP Specialists: warning letter of May 12, 2005
FDA warning letter UCM075404 · Los Angeles District Office
Key facts
| Reference number | UCM075404 |
|---|---|
| Company | C & E GP Specialists |
| Subject | Quality System Regulations (QSR) for finished devices/adulterated |
| Issue date | May 12, 2005 |
| Posted date | May 12, 2005 |
| Issuing office | Los Angeles District Office |
| Product type | Devices |
| Country | 3 |
| Inspection city | San Diego |
| Inspection ZIP | 92127-1828 |
| Inspection start date | Jan 26, 2005 |
| Letter on fda.gov | web.archive.org |
At a glance
- 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: