Warning letter
Dandy Day Corporation: warning letter of Dec 17, 2014
FDA warning letter 434419 · Denver District Office
Key facts
| Reference number | 434419 |
|---|---|
| Company | Dandy Day Corporation |
| Subject | CGMP/Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements/Adulterated |
| Issue date | Dec 17, 2014 |
| Posted date | Dec 30, 2014 |
| Issuing office | Denver District Office |
| Product type | Food/Cosmetics |
| CFR sections cited | 101.36, 111, 111.70, 111.95, 111.103, 111.135, 111.210, 111.260, 101.36(b)(1)(ii), 101.36(e)(1), 101.4(a), 101.9(b) and 26 more |
| Inspection city | Montrose |
| Inspection ZIP | 81401 |
| Inspection start date | Apr 2, 2014 |
| 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: