Warning letter
Med-Mizer, Inc.: warning letter of Jul 21, 2014
FDA warning letter 423788 · Detroit District Office
Key facts
| Reference number | 423788 |
|---|---|
| Company | Med-Mizer, Inc. |
| Subject | CGMP/QSR/Medical Devices/Adulterated |
| Issue date | Jul 21, 2014 |
| Posted date | Jul 29, 2014 |
| Issuing office | Detroit District Office |
| Product type | Devices |
| CFR sections cited | 803, 803.17, 806, 806.10, 803.50(a)(1), 820 |
| Inspection city | Batesville |
| Inspection ZIP | 47006 |
| Inspection start date | Feb 19, 2014 |
| 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: