Warning letter
Intercos Europe S.p.A: warning letter of Aug 15, 2024
FDA warning letter 682273 · Center for Drug Evaluation and Research (CDER)
Key facts
| Reference number | 682273 |
|---|---|
| Company | Intercos Europe S.p.A |
| Subject | CGMP/Finished Pharmaceuticals/Adulterated |
| Issue date | Aug 15, 2024 |
| Posted date | Aug 20, 2024 |
| Issuing office | Center for Drug Evaluation and Research (CDER) |
| Product type | Drugs |
| CFR sections cited | 211.194(a), 211.192, 211.84(d)(1), 211.34 |
| Inspection city | Agrate Brianza |
| Inspection start date | Mar 11, 2024 |
| 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: