Warning letter
Misonix, Inc.: warning letter of Dec 20, 2001
FDA warning letter UCM178443 · Denver District Office
Key facts
| Reference number | UCM178443 |
|---|---|
| Company | Misonix, Inc. |
| Subject | GMP Requirements for the Quality System Regulation/Adulterated |
| Issue date | Dec 20, 2001 |
| Posted date | Dec 20, 2001 |
| Issuing office | Denver District Office |
| Product type | Devices |
| CFR sections cited | 820 |
| Country | 3 |
| Letter on fda.gov | web.archive.org |
At a glance
- 1–9 CFR sections cited
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: