French data is current through early September 2018. All of the data comes from L’Agence nationale de sécurité du médicament et des produits de santé (ANSM), except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and France.
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Following an inspection conducted by the ANSM, the company Adgenix informed the users of the Cytomax culture medium of the withdrawal of this product. The users concerned have received the attached mail (16/09/2015) (137 KB).