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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
112-8456087-7/1/1 25-Oct-2005 57DY03 3004839613 Zlb Behring Gmbh Germany
 
112-8627782-7/1/1 25-Oct-2005 57GC01 3004505311 Breakspear Medical United Kingdom
 
FR1-0011307-0/1/1 06-Oct-2005 57YH02 3003279193 Amsino Medical Instrument Co Ltd China
 
FR1-0011314-6/1/1 06-Oct-2005 57YH02 3003279193 Amsino Medical Instrument Co Ltd China
 
112-8461854-3/1/1 24-Oct-2005 57YY99 3004948405 Wamex Diagnostics Canada
 
112-8372157-9/1/1 25-Oct-2005 57YY99 3004091344 Dna Genotek Inc Canada
 
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