• 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
110-0835683-5/1/1 06-Feb-2007 57DC19 1000609485 Shinonogi And Company Ltd Japan
 
AD1-0326845-5/23/1 20-Feb-2007 57GB01 3003863312 Naturals Distributing Inc Canada
 
802-0018055-4/1/1 13-Feb-2007 57HC42 3002580567 Wyeth Pharmaceuticals, Ltd United Kingdom
 
-
-