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Negócios · 19/06/19981 min de leitura
Knickerbocker Biologicals, Inc.; Revocation of U.S. License No. 458-001
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Resumo
The Food and Drug Administration (FDA) is announcing the revocation of the establishment license (U.S. License No. 458-001) and the product licenses issued to Knickerbocker Biologicals, Inc., for the manufacture of Whole Blood, Red Blood Cells, Plasma, and Source Leukocytes. Knickerbocker Biologicals, 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 →