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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
112-0016753-5/1/1 29-Mar-2002 57JH03 3003597491 Tutogen Medical Gmbh Germany
 
112-0475821-2/1/1 27-Mar-2002 57MY01 3003592680 Musgrove Park Hopital United Kingdom
 
110-8205188-9/1/1 01-Mar-2002 57YY01 3003591523 Faculdade De Medicina U.S.P. Brazil
 
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