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U.S. Department of Health and Human Services

Import Refusal Report

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Refusal Details as Recorded in OASIS by FDA

for Refusal W92-0164494-0/1/1


Manufacturer FEI3006770240
Manufacturer NameChang Jo Int'L Co., Ltd  
Manufacturer Address line 158-38, CHONGCHON-DONG , BUPYEONG-GU  
Manufacturer Address line 2  
Manufacturer's CityIncheon  
Manufacturer Province/StateINCHEON GWANGYEOGSIV  
Manufacturer Country/AreaKorea, Republic Of (South)  
Product Code89ISA  
Importer's Product DescriptionNURIEYE EYE MASSAGER  
Refusal Date19-Aug-2010  
FDA DistrictLOS-DO  
Entry/doc/line/sfx W92-0164494-0/1/1
FDA Sample AnalysisNo  
FDA Record of Private Lab Sample Analysis No  
Charge(s)
Violation Code Section Charge Statement
FALSE   502(a), 801(a)(3); MISBRANDING   The labeling for this article appears to be false or misleading  
NOT LISTED   502(o), 801(a)(3); MISBRANDING   It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).  
REGISTERED   502(o), 801(a)(3); MISBRANDING   It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).  
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