Warning letter
Wholistic Herbs, Inc.: warning letter of Oct 5, 2012
FDA warning letter 300998 · Dallas District Office
Key facts
| Reference number | 300998 |
|---|---|
| Company | Wholistic Herbs, Inc. |
| Subject | CGMP/Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements/Adulterated |
| Issue date | Oct 5, 2012 |
| Posted date | Oct 5, 2012 |
| Issuing office | Dallas District Office |
| Product type | Food/Cosmetics |
| CFR sections cited | 101.36, 111, 111.83, 111.103, 111.210, 111.260, 111.503, 111.510, 111.553, 101.3(g), 101.4(g), 111.13(a) and 10 more |
| Inspection city | Dallas |
| Inspection ZIP | 75230 |
| Inspection start date | Dec 28, 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: