Warning letter
Threshold Enterprises Ltd: warning letter of Oct 12, 2016
FDA warning letter 499200 · San Francisco District Office
Key facts
| Reference number | 499200 |
|---|---|
| Company | Threshold Enterprises Ltd |
| Subject | CGMP/Dietary Supplement/Adulterated/Misbranded |
| Issue date | Oct 12, 2016 |
| Posted date | Oct 12, 2016 |
| Issuing office | San Francisco District Office |
| Product type | Food/Cosmetics |
| CFR sections cited | 310.530(b), 111, 111.73, 101.4(a), 101.4(g), 101.4(h), 101.9(b), 111.70(b), 111.70(b)(1), 111.70(b)(2), 111.70(b)(3), 111.70(c)(2) and 4 more |
| Inspection city | Scotts Valley |
| Inspection ZIP | 95066 |
| Inspection start date | Mar 21, 2016 |
| 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: