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U.S. Department of Health and Human Services

Import Refusal Report

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Refusal Actions by FDA as Recorded in OASIS

for 80-General Hospital/Personal Use


Entry/doc/line/sfx Refusal Date Product
Code
Manufacturer
FEI
Manufacturer
Name
Manufacturer
Country/Area
DQ1-0129293-5/4/1 03-Dec-2002 80FLK 3003667324 Ends Corporation Taiwan
 
DQ1-0129293-5/5/1 03-Dec-2002 80FLL 3003667324 Ends Corporation Taiwan
 
399-0910285-5/1/2 04-Dec-2002 80FMC 3003662661 Cymun Development Sdn Bhd Malaysia
 
582-0243173-0/3/1 05-Dec-2002 80FMC 3003165446 Eikon Device Inc Canada
 
224-0332087-6/1/7 03-Dec-2002 80FMF 1118880 Terumo Medical Corporation United States
 
F11-1955312-3/1/2 20-Dec-2002 80JOK 5471 House Of Surgical Pakistan
 
EQ6-0002546-2/1/1 27-Dec-2002 80JOK 6078 Aesculap Werk Aktiengesellschaft Germany
 
582-0243173-0/4/1 05-Dec-2002 80LDQ 3003165446 Eikon Device Inc Canada
 
XXX-0056274-5/3/1 13-Dec-2002 80LDQ 3003871466 Finesun Electric Co Ltd Taiwan
 
582-0086630-9/1/1 11-Dec-2002 80LJS 3002584707 Meditron, Inc. Canada
 
427-1160677-4/1/1 10-Dec-2002 80MXI 3003826265 Hwangto & Namu Co., Ltd. Korea, Republic Of (South)
 
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