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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
112-0629701-3/1/1 08-May-2002 57DB14 1000309874 International Pharmacy Organsation United Kingdom
 
582-0005106-8/1/1 28-May-2002 57DI19 1000135102 Cliniqa Corp United States
 
336-1289317-4/1/1 15-May-2002 57DY03 1000271192 Baxter Medical Ab Sweden
 
110-8077076-1/2/1 01-May-2002 57YY99 3001190779 Mcewen Laboratories Limited United Kingdom
 
110-8079430-8/2/1 01-May-2002 57YY99 3001190779 Mcewen Laboratories Limited United Kingdom
 
110-8079402-7/2/1 01-May-2002 57YY99 3001190779 Mcewen Laboratories Limited United Kingdom
 
110-8081085-6/1/1 03-May-2002 57YY99 3001190779 Mcewen Laboratories Limited United Kingdom
 
110-8081085-6/2/1 03-May-2002 57YY99 3001190779 Mcewen Laboratories Limited United Kingdom
 
110-8077354-2/1/1 10-May-2002 57YY99 3001190779 Mcewen Laboratories Limited United Kingdom
 
110-8153591-6/1/1 16-May-2002 57YY99 3001190779 Mcewen Laboratories Limited United Kingdom
 
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