Warning letter
Nutri-Dyn Midwest, Inc.: warning letter of Jan 15, 2016
FDA warning letter 461006 · Minneapolis District Office
Key facts
| Reference number | 461006 |
|---|---|
| Company | Nutri-Dyn Midwest, Inc. |
| Subject | New Drugs/Dietary Supplements/Labeling/Misbranded/Adulterated |
| Issue date | Jan 15, 2016 |
| Posted date | Jan 25, 2016 |
| Issuing office | Minneapolis District Office |
| Product type | Food/Cosmetics |
| CFR sections cited | 111.127(h), 111, 111.55, 111.103, 111.105, 111.70(e), 111.560(a)(2), 111.570(b)(1), 111.75(c), 111.75(c)(3), 201.5, 207 |
| Inspection city | Maple Plain |
| Inspection ZIP | 55359 |
| Inspection start date | Mar 24, 2015 |
| 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: