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U.S. Department of Health and Human Services

Import Refusal Report

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Refusal Actions by FDA as Recorded in OASIS

for 57-Bio & Licensed In-Vivo & In-Vitro Diag


Entry/doc/line/sfx Refusal Date Product
Code
Manufacturer
FEI
Manufacturer
Name
Manufacturer
Country/Area
233-2841622-9/1/1 25-Jun-2003 57CY02 3002808087 Schering-Plough (Brinny) Co. Ireland
 
MC2-0077120-2/1/1 23-Jun-2003 57JH01 3002487675 Tutogen Medical Gmbh Germany
 
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