• 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 90-Radiological


Entry/doc/line/sfx Refusal Date Product
Code
Manufacturer
FEI
Manufacturer
Name
Manufacturer
Country/Area
112-1174606-5/1/1 23-Aug-2011 90ITX 3001701594 Protek Medical Products Inc United States
 
112-0935898-0/1/1 23-Aug-2011 90ITX 3002957361 Medical Measurement Systems B.V. Netherlands
 
112-7085938-6/1/1 19-Aug-2011 90IYN 3006225101 Ultrasonix Medical Corporation Canada
 
112-3365473-5/1/1 25-Aug-2011 90IYX 3002902882 Applied Scintillation Technologies United Kingdom
 
M76-1528613-7/1/1 18-Aug-2011 90IZL 1000316700 Sterne Manafacturing Canada
 
M76-1528613-7/2/1 18-Aug-2011 90IZL 1000316700 Sterne Manafacturing Canada
 
M76-1528613-7/4/1 18-Aug-2011 90IZL 1000316700 Sterne Manafacturing Canada
 
U35-1990954-3/1/1 25-Aug-2011 90JAK 1000506423 Ge Medical Systems United States
 
U35-1991274-5/1/1 25-Aug-2011 90JAK 1000506423 Ge Medical Systems United States
 
T94-0055686-4/1/1 03-Aug-2011 90LLZ 3008506621 Carestream Health Hong Kong SAR
 
-
-