Warning letter
Samson Pharmaceuticals, Inc: warning letter of Dec 13, 2018
FDA warning letter 554307 · Center for Drug Evaluation and Research
Key facts
| Reference number | 554307 |
|---|---|
| Company | Samson Pharmaceuticals, Inc |
| Subject | CGMP/Finished Pharmaceuticals/Adulterated |
| Issue date | Dec 13, 2018 |
| Posted date | Feb 12, 2019 |
| Issuing office | Center for Drug Evaluation and Research |
| Product type | Drugs |
| CFR sections cited | 211.165(e), 211.166(a), 211.84(d)(1), 211.34, 211.42(c)(10)(i), 211.42(c)(10)(iv), 211.113(b) |
| Inspection city | Commerce |
| Inspection ZIP | 90040 |
| Inspection start date | Jan 24, 2018 |
| Letter on fda.gov | fda.gov |
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: