Warning letter
Cenova Innovation and Productions AB [ARCHIVED]: warning letter of Feb 25, 2011
FDA warning letter 158492 · Center for Devices and Radiological Health
Key facts
| Reference number | 158492 |
|---|---|
| Company | Cenova Innovation and Productions AB [ARCHIVED] |
| Subject | CGMP/QSR/Manufacture/Packing/Storage/Installation/Adulterated |
| Issue date | Feb 25, 2011 |
| Posted date | Feb 25, 2011 |
| Issuing office | Center for Devices and Radiological Health |
| Product type | Devices |
| CFR sections cited | 820 |
| 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: