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Negocios · 5/8/19971 min de lectura
Personal Blood Storage of Memphis, Inc.; Revocation of U.S. License No. 1131
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Resumen
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 de la fuente: Federal Register — Food and Drug AdministrationAbrir el comunicado original →