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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
310-9137721-3/1/1 05-Dec-2003 57CC11 3002972083 Sanofi Pasteur SA France
 
582-6571794-2/1/1 24-Dec-2003 57DY14 3000316593 NORWICKY PHARMA Austria
 
112-1507023-6/2/1 03-Dec-2003 57DY24 3002733826 Sistema Sviluppo Servizi Srl Italy
 
112-1531385-9/1/1 18-Dec-2003 57FY88 3001633962 Novocastra Labs Ltd United Kingdom
 
112-1920711-5/1/1 15-Dec-2003 57YY99 3003804235 Cypress Diagnostics Belgium
 
112-1990252-5/1/1 17-Dec-2003 57YY99 3003538383 All Diag Sa France
 
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