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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 90-Radiological


Entry/doc/line/sfx Refusal Date Product
Code
Manufacturer
FEI
Manufacturer
Name
Manufacturer
Country/Area
112-7227634-0/1/1 14-Jun-2010 90ITX 3019216 Philips Ultrasound, Inc. United States
 
MC2-6188939-8/2/1 24-Jun-2010 90IYO 3002807409 Kontron Instruments Sa France
 
MC2-6188939-8/6/1 24-Jun-2010 90IYO 3002807409 Kontron Instruments Sa France
 
E9G-1006890-5/1/1 15-Jun-2010 90MQB 3003840967 Edge Medical Device Ltd Israel
 
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