Warning letter
Qingdao Jiulong Biopharmaceuticals Co. Ltd. [ARCHIVED]: warning letter of Apr 14, 2009
FDA warning letter 56042 · Center for Drug Evaluation and Research
Key facts
| Reference number | 56042 |
|---|---|
| Company | Qingdao Jiulong Biopharmaceuticals Co. Ltd. [ARCHIVED] |
| Subject | CGMP Requirements in the Manufacturing of Drugs/Adulterated |
| Issue date | Apr 14, 2009 |
| Posted date | Apr 14, 2009 |
| Issuing office | Center for Drug Evaluation and Research |
| Product type | Drugs |
| Inspection city | Qingdao |
| Inspection start date | Jul 28, 2008 |
| Letter on fda.gov | web.archive.org |
At a glance
- 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: