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Talk to a SpecialistTalk to a SpecialistCDL Services, Inc. DBA Technichem, a manufacturer of over-the-counter hand sanitizers and hand soap, violated Current Good Manufacturing Practice (CGMP) regulations by failing to perform adequate laboratory testing on finished drug products before release to the market. During an FDA inspection in April 2025, investigators found that the company had not tested batches for identity and strength of active ingredients (such as ethanol and chloroxylenol) for over a year, instead relying on simulated testing results, which rendered the drug products adulterated under federal law. The firm's failure to ensure satisfactory conformance to final specifications prior to distribution represented a significant violation of 21 CFR 211.165(a).