Warning letter
Vitalab Co Inc: warning letter of Oct 16, 2014
FDA warning letter 432743 · Kansas City District Office
Key facts
| Reference number | 432743 |
|---|---|
| Company | Vitalab Co Inc |
| Subject | CGMP/Unapproved New Drugs/Dietary Supplements/Adulterated/Misbranding/Labeling |
| Issue date | Oct 16, 2014 |
| Posted date | Oct 28, 2014 |
| Issuing office | Kansas City District Office |
| Product type | Food/Cosmetics |
| CFR sections cited | 111.570(b)(2)(ii), 101, 101.4, 111, 111.73, 111.103, 111.105, 111.153, 111.170, 111.210, 111.570, 111.12(c) and 10 more |
| Inspection city | Liberty |
| Inspection ZIP | 64068 |
| Inspection start date | May 8, 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: