Warning letter
Ortho Molecular Products Inc: warning letter of Oct 15, 2012
FDA warning letter 308738 · Minneapolis District Office
Key facts
| Reference number | 308738 |
|---|---|
| Company | Ortho Molecular Products Inc |
| Subject | New Drug/Labeling/Misbranded |
| Issue date | Oct 15, 2012 |
| Posted date | Oct 15, 2012 |
| Issuing office | Minneapolis District Office |
| Product type | Food/Cosmetics |
| Inspection city | Stevens Point |
| Inspection ZIP | 54482 |
| Inspection start date | Apr 3, 2012 |
| 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: