Warning letter
Vertebral Technologies, Inc.: warning letter of Sep 4, 2015
FDA warning letter 453675 · Minneapolis District Office
Key facts
| Reference number | 453675 |
|---|---|
| Company | Vertebral Technologies, Inc. |
| Subject | Medical Device Reporting/Misbranded |
| Issue date | Sep 4, 2015 |
| Posted date | Sep 28, 2015 |
| Issuing office | Minneapolis District Office |
| Product type | Devices |
| CFR sections cited | 803.3, 803.17(a), 803.50(a), 803, 803.50(a)(2) |
| Inspection city | Santa Clara |
| Inspection ZIP | 95051 |
| Inspection start date | Jan 28, 2015 |
| 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: