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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
112-3871991-7/1/1 18-Aug-2003 57AY02 1000493316 Allergan Canada Canada
 
112-1073279-8/1/1 26-Aug-2003 57HY81 3004080150 Dr.Andrew Wakefield United Kingdom
 
112-0656958-4/1/1 12-Aug-2003 57YY99 3002546385 Trinity Biotech Plc Ireland
 
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