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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
112-7949753-0/1/1 10-Dec-2005 57CC02 3004547032 Gemeinschaftspraxis Rohle/Schwen Germany
 
112-8322114-0/1/1 14-Dec-2005 57DK49 2020808 Scantibodies Laboratory, Inc. United States
 
FR1-0011363-3/1/1 27-Dec-2005 57YH02 3003279193 Amsino Medical Instrument Co Ltd China
 
FR1-0011386-4/1/1 27-Dec-2005 57YH02 3003279193 Amsino Medical Instrument Co Ltd China
 
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