Warning letter
PurQuality, LLC: warning letter of Dec 4, 2013
FDA warning letter 394584 · Los Angeles District Office
Key facts
| Reference number | 394584 |
|---|---|
| Company | PurQuality, LLC |
| Subject | CGMP/Dietary Supplement/Adulterated/Misbranded |
| Issue date | Dec 4, 2013 |
| Posted date | Dec 4, 2013 |
| Issuing office | Los Angeles District Office |
| Product type | Food/Cosmetics |
| CFR sections cited | 111.75(a)(2)(ii), 111.75(a), 101.36(b)(3), 111.110(c), 111.123(a)(7), 111, 111.75, 101.36(b)(1)(ii), 111.70(e) |
| Inspection city | Tempe |
| Inspection ZIP | 85281 |
| Inspection start date | Jan 14, 2013 |
| Letter on fda.gov | web.archive.org |
At a glance
- 1–9 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: