• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Import Refusal Report

  • Print
  • Share
  • E-mail
-

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
FR1-0011185-0/1/1 10-Jun-2005 57YH02 3003279193 Amsino Medical Instrument Co Ltd China
 
FR1-0011210-6/1/1 10-Jun-2005 57YH02 3003279193 Amsino Medical Instrument Co Ltd China
 
FR1-0011235-3/1/1 17-Jun-2005 57YH02 3003279193 Amsino Medical Instrument Co Ltd China
 
FR1-0011248-6/1/1 21-Jun-2005 57YH02 3000247873 Nipro Corporation Japan
 
112-6827125-1/1/1 28-Jun-2005 57YY99 3003453957 Technoclone Gmbh Austria
 
112-6679066-6/1/1 29-Jun-2005 57YY99 3005082212 Technoclone Ges Austria
 
-
-