Warning letter
TEFTEC Corporation: warning letter of Apr 24, 2006
FDA warning letter UCM075877 · Dallas District Office
Key facts
| Reference number | UCM075877 |
|---|---|
| Company | TEFTEC Corporation |
| Subject | CGMP for Medical Device Reporting/Adulterated |
| Issue date | Apr 24, 2006 |
| Posted date | Apr 24, 2006 |
| Issuing office | Dallas District Office |
| Product type | Devices |
| CFR sections cited | 803, 803.17, 803.18, 820 |
| Country | 3 |
| Inspection city | San Antonio |
| Inspection ZIP | 78249-3341 |
| Inspection start date | Feb 6, 2006 |
| Letter on fda.gov | web.archive.org |
At a glance
- 1–9 CFR sections cited
- 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: