Warning letter
CDL Services, Inc. DBA Technichem: warning letter of Nov 24, 2025
FDA warning letter 713877 · Center for Drug Evaluation and Research (CDER)
Key facts
| Reference number | 713877 |
|---|---|
| Company | CDL Services, Inc. DBA Technichem |
| Subject | CGMP/Finished Pharmaceuticals/Adulterated |
| Issue date | Nov 24, 2025 |
| Posted date | Dec 9, 2025 |
| Issuing office | Center for Drug Evaluation and Research (CDER) |
| Product type | Drugs |
| CFR sections cited | 211.137(a), 211.188(b), 211.22, 211.22(a), 211.34, 211.68(b), 211.84(d)(1), 211.100(a), 211.165(a) |
| Inspection city | Anaheim |
| Inspection ZIP | 92806 |
| Inspection start date | Apr 7, 2025 |
| Letter on fda.gov | fda.gov |
At a glance
- 1–9 CFR sections cited
- OAI Linked inspection classification
- Yes Form FDA 483 issued
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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: