Warning letter
Teco Diagnostics [ARCHIVED]: warning letter of Aug 20, 2010
FDA warning letter 113248 · Los Angeles District Office
Key facts
| Reference number | 113248 |
|---|---|
| Company | Teco Diagnostics [ARCHIVED] |
| Subject | CGMP/QSR/Manufacture/Packing/Storage/Installation/Adulterated |
| Issue date | Aug 20, 2010 |
| Posted date | Aug 20, 2010 |
| Issuing office | Los Angeles District Office |
| Product type | Devices |
| CFR sections cited | 807.81(b), 820 |
| Inspection city | Anaheim |
| Inspection ZIP | 92807 |
| Inspection start date | Mar 24, 2010 |
| 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: