Warning letter
CTX Lifesciences Private Ltd.: warning letter of Jul 12, 2019
FDA warning letter 577416 · Center for Drug Evaluation and Research
Key facts
| Reference number | 577416 |
|---|---|
| Company | CTX Lifesciences Private Ltd. |
| Subject | CGMP/Active Pharmaceutical Ingredient (API)/Adulterated |
| Issue date | Jul 12, 2019 |
| Posted date | Aug 27, 2019 |
| Issuing office | Center for Drug Evaluation and Research |
| Product type | Drugs |
| CFR sections cited | 211.192 |
| Inspection city | Surat |
| Inspection start date | Feb 11, 2019 |
| 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: