Warning letter
MedTec Inc: warning letter of Jun 28, 2005
FDA warning letter UCM075467 · Kansas City District Office
Key facts
| Reference number | UCM075467 |
|---|---|
| Company | MedTec Inc |
| Subject | QSR/Medical Devices/Adulterated |
| Issue date | Jun 28, 2005 |
| Posted date | Jun 28, 2005 |
| Issuing office | Kansas City District Office |
| Product type | Devices |
| Country | 3 |
| Inspection city | Orange City |
| Inspection ZIP | 51041-7463 |
| Inspection start date | Apr 25, 2005 |
| Letter on fda.gov | web.archive.org |
At a glance
- 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: