Warning letter
VertiFlex, Inc. [ARCHIVED]: warning letter of Jul 14, 2010
FDA warning letter 106585 · Los Angeles District Office
Key facts
| Reference number | 106585 |
|---|---|
| Company | VertiFlex, Inc. [ARCHIVED] |
| Subject | Premarket Approval/Adulterated |
| Issue date | Jul 14, 2010 |
| Posted date | Jul 14, 2010 |
| Issuing office | Los Angeles District Office |
| Product type | Devices |
| CFR sections cited | 803, 803.50(a) |
| Inspection city | Carlsbad |
| Inspection ZIP | 92010 |
| Inspection start date | Feb 2, 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: