Warning letter
Innovative Med Inc.: warning letter of Mar 19, 2013
FDA warning letter 372459 · Los Angeles District Office
Key facts
| Reference number | 372459 |
|---|---|
| Company | Innovative Med Inc. |
| Subject | CGMP/QSR/Medical Devices/Adulterated |
| Issue date | Mar 19, 2013 |
| Posted date | Mar 19, 2013 |
| Issuing office | Los Angeles District Office |
| Product type | Devices |
| CFR sections cited | 801.4, 807.81(b), 890.9, 890.5660 |
| Inspection city | Irvine |
| Inspection ZIP | 92618 |
| Inspection start date | Oct 3, 2012 |
| 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: