Warning letter
Genetics & IVF Institute [ARCHIVED]: warning letter of Nov 20, 2009
FDA warning letter UCM193908 · Center for Devices and Radiological Health
Key facts
| Reference number | UCM193908 |
|---|---|
| Company | Genetics & IVF Institute [ARCHIVED] |
| Subject | Sponsor/Monitor/Contract Research Organization |
| Issue date | Nov 20, 2009 |
| Posted date | Nov 20, 2009 |
| Issuing office | Center for Devices and Radiological Health |
| Product type | Devices |
| CFR sections cited | 812.140(b)(1), 50.27(a), 812.40, 812.100, 812.25(e), 812.46(a) |
| Country | 3 |
| Letter on fda.gov | web.archive.org |
At a glance
- 1–9 CFR sections cited
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: