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PubMed: 17934097

FDA investigators found that drug products produced failed to meet the conditions of Section 503A of the FDCA, including that Foothills did not receive valid prescriptions for individually identified patients for a portion of the drug products produced, and that investigators noted serious deficiencies in drug production practices that put patients at risk

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Forma parte del perfil farmacolgico combinado descrito en ensayos de activacin celular