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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
112-8019023-1/2/1 28-Nov-2005 57FB28 3004910133 Diamed AG Switzerland
 
110-2542482-5/1/1 10-Nov-2005 57FY56 3004758118 Merck & Co Inc United States
 
MC2-0088455-9/1/1 30-Nov-2005 57JH01 3002487675 Tutogen Medical Gmbh Germany
 
MC2-0088456-7/1/1 30-Nov-2005 57JH01 3002487675 Tutogen Medical Gmbh Germany
 
112-8764547-7/1/1 04-Nov-2005 57OJ02 3003773152 Euroscreen Belgium
 
FR1-0011343-5/1/1 01-Nov-2005 57YH02 3003279193 Amsino Medical Instrument Co Ltd China
 
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