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Entreprise · 05/08/19971 min de lecture
Personal Blood Storage of Memphis, Inc.; Revocation of U.S. License No. 1131
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Résumé
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.
Langue originale de la source: Federal Register — Food and Drug AdministrationOuvrir le communiqué original →