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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
XXX-0045406-7/3/1 02-Apr-2002 57FY55 3003606065 Diagnostic Product Corporation United States
 
110-7987271-9/2/1 08-Apr-2002 57GB01 3001190779 Mcewen Laboratories Limited United Kingdom
 
110-7987250-3/2/1 03-Apr-2002 57GF01 3001190779 Mcewen Laboratories Limited United Kingdom
 
DR7-0001641-0/1/1 16-Apr-2002 57YY02 3003606202 Nipro Medical Corp Chile Chile
 
112-0037275-4/1/1 01-Apr-2002 57YY99 3001190779 Mcewen Laboratories Limited United Kingdom
 
112-0037275-4/2/1 01-Apr-2002 57YY99 3001190779 Mcewen Laboratories Limited United Kingdom
 
110-7998431-6/1/1 08-Apr-2002 57YY99 1000230999 Kings College Hospital United Kingdom
 
112-0066043-0/1/1 30-Apr-2002 57YY99 3002821759 Health Angel GMBH Switzerland
 
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