Warning letter
TZ Medical, Inc.: warning letter of Feb 2, 2006
FDA warning letter UCM075787 · Seattle District Office
Key facts
| Reference number | UCM075787 |
|---|---|
| Company | TZ Medical, Inc. |
| Subject | Lacks Premarket Approval Application Misbranded |
| Issue date | Feb 2, 2006 |
| Posted date | Feb 2, 2006 |
| Issuing office | Seattle District Office |
| Product type | Devices |
| CFR sections cited | 807.81(a)(3)(i), 807.81(b) |
| Country | 3 |
| Inspection city | Portland |
| Inspection ZIP | 97224-7086 |
| Inspection start date | Aug 22, 2005 |
| 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: