Warning letter
Silgan Dispensing Systems: warning letter of Oct 5, 2026
FDA warning letter 734538 · Center for Drug Evaluation and Research (CDER)
Key facts
| Reference number | 734538 |
|---|---|
| Company | Silgan Dispensing Systems |
| Subject | CGMP/Finished Pharmaceuticals/Adulterated/Unapproved New Drug |
| Issue date | Oct 5, 2026 |
| Posted date | Oct 13, 2026 |
| Issuing office | Center for Drug Evaluation and Research (CDER) |
| Product type | Drugs |
| CFR sections cited | 211.180(e), 201.128, 211.22, 211.34, 211.84(d)(2), 211.166(a), 211.192 |
| Inspection city | Spokane |
| Inspection ZIP | 99224-5326 |
| Inspection start date | Mar 26, 2026 |
| Letter on fda.gov | fda.gov |
At a glance
- 1–9 CFR sections cited
- 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: