Warning letter
VUAB Pharma a.s.: warning letter of May 27, 2015
FDA warning letter 441838 · Center for Drug Evaluation and Research
Key facts
| Reference number | 441838 |
|---|---|
| Company | VUAB Pharma a.s. |
| Subject | CGMP/Active Pharmaceutical Ingredient (API)/Adulterated |
| Issue date | May 27, 2015 |
| Posted date | Jun 2, 2015 |
| Issuing office | Center for Drug Evaluation and Research |
| Product type | Drugs |
| Inspection city | Roztoky |
| Inspection start date | Jun 9, 2014 |
| 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: