• 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
112-7935104-3/1/1 22-Aug-2005 57GB01 3002096442 Chemotechnique Diagnostics Sweden
 
FR1-0011282-5/1/1 12-Aug-2005 57YH02 3003279193 Amsino Medical Instrument Co Ltd China
 
-
-