Warning letter
Guangdong Zhanjiang Jimin Pharmaceutical Co., Ltd.: warning letter of Oct 30, 2017
FDA warning letter 534215 · Center for Drug Evaluation and Research
Key facts
| Reference number | 534215 |
|---|---|
| Company | Guangdong Zhanjiang Jimin Pharmaceutical Co., Ltd. |
| Subject | CGMP/Finished Pharmaceuticals/Adulterated |
| Issue date | Oct 30, 2017 |
| Posted date | Nov 7, 2017 |
| Issuing office | Center for Drug Evaluation and Research |
| Product type | Drugs |
| CFR sections cited | 211.165(a), 330.10(a)(12), 211.34, 330.1, 211.22(a), 211.100(a) |
| Inspection city | Zhangjiang |
| Inspection start date | May 15, 2017 |
| 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: