Warning letter
Neoventa Medical AB [ARCHIVED]: warning letter of Aug 4, 2010
FDA warning letter 120669 · Center for Devices and Radiological Health
Key facts
| Reference number | 120669 |
|---|---|
| Company | Neoventa Medical AB [ARCHIVED] |
| Subject | CGMP/QSR/Medical Devices/Adulterated/Misbranded |
| Issue date | Aug 4, 2010 |
| Posted date | Aug 4, 2010 |
| Issuing office | Center for Devices and Radiological Health |
| Product type | Devices |
| CFR sections cited | 21, 20.90(b)(2), 803, 803.3, 803.17(a)(1), 803.50(a)(1), 820, 820.3(b) |
| Inspection city | Molndal |
| Inspection start date | Mar 29, 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: