Warning letter
Vulcon Technologies Inc [ARCHIVED]: warning letter of Mar 17, 2010
FDA warning letter 81184 · Center for Devices and Radiological Health
Key facts
| Reference number | 81184 |
|---|---|
| Company | Vulcon Technologies Inc [ARCHIVED] |
| Subject | Device/Misbranded |
| Issue date | Mar 17, 2010 |
| Posted date | Mar 17, 2010 |
| Issuing office | Center for Devices and Radiological Health |
| Product type | Devices |
| Inspection city | Grandview |
| Inspection ZIP | 64030 |
| Inspection start date | Jul 1, 2009 |
| Letter on fda.gov | web.archive.org |
At a glance
- VAI 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: