• 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 84-Neurological


Entry/doc/line/sfx Refusal Date Product
Code
Manufacturer
FEI
Manufacturer
Name
Manufacturer
Country/Area
112-1030445-2/1/1 27-May-2011 84GWQ 3008308153 Deymed Diagnostic S.R.O Czech Republic
 
112-1030445-2/2/1 27-May-2011 84GWQ 3008308153 Deymed Diagnostic S.R.O Czech Republic
 
-
-