Warning letter
HoneyCombs Industries, LLC: warning letter of Feb 24, 2016
FDA warning letter 481691 · Denver District Office
Key facts
| Reference number | 481691 |
|---|---|
| Company | HoneyCombs Industries, LLC |
| Subject | CGMP/Dietary Supplement/Adulterated/Misbranded |
| Issue date | Feb 24, 2016 |
| Posted date | Mar 8, 2016 |
| Issuing office | Denver District Office |
| Product type | Food/Cosmetics |
| CFR sections cited | 111.210(h)(3), 111, 111.70, 111.73, 111.75, 111.103, 111.255, 111.260, 101.3(g), 111.25(c), 111.35(b)(2), 111.70(b) and 11 more |
| Inspection city | Montrose |
| Inspection ZIP | 81403 |
| Inspection start date | Jul 7, 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: