Warning letter
Modern Products, Inc.: warning letter of Mar 7, 2012
FDA warning letter 236774 · Minneapolis District Office
Key facts
| Reference number | 236774 |
|---|---|
| Company | Modern Products, Inc. |
| Subject | CGMP/Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements/Adulterated |
| Issue date | Mar 7, 2012 |
| Posted date | Mar 7, 2012 |
| Issuing office | Minneapolis District Office |
| Product type | Food/Cosmetics |
| CFR sections cited | 111.415, 101, 111, 111.103, 111.403, 111.453, 101.9, 101.9(b), 101.9(b)(9), 101.9(c)(8)(ii), 111.70(f), 111.430(b) and 4 more |
| Inspection city | Mequon |
| Inspection ZIP | 53092 |
| Inspection start date | Aug 16, 2011 |
| Letter on fda.gov | web.archive.org |
At a glance
- 10–99 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: