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Regulatorische Updates24. Aug. 2026•1 Min. Lesezeit

FDA Recalls Product Due to CGMP Deviations

Vom PharmaCountry-Team

The FDA has initiated a recall of a product because of deviations from current Good Manufacturing Practices (CGMP).

The U.S. Food and Drug Administration (FDA) has issued a recall for a pharmaceutical product after identifying deviations from current Good Manufacturing Practices (CGMP). The recall underscores the agency's focus on ensuring manufacturing compliance and product safety.

Zusammengestellt vom PharmaCountry-Team · Quelle: FDA.gov