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Negócios · 05/08/19971 min de leitura
Personal Blood Storage of Memphis, Inc.; Revocation of U.S. License No. 1131
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Resumo
The Food and Drug Administration (FDA) is announcing the revocation of the establishment license (U.S. License No. 1131) and the product licenses issued to Personal Blood Storage of Memphis, Inc., for the manufacture of Whole Blood, Red Blood Cells, Plasma, and Platelets. Personal Blood Storage of Memphis, Inc., did not respond to a notice of opportunity for a hearing on a proposal to revoke its licenses.
Idioma original da fonte: Federal Register — Food and Drug AdministrationAbrir o comunicado original →