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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 551-9507121-7/1/1

Manufacturer FEI1000215072
Manufacturer NameMelong Products Factory  
Manufacturer Address line 1Block 3 Hanji Ind Estate  
Manufacturer Address line 2Hanji Town  
Manufacturer's CityShenzhen  
Manufacturer Province/StateGUANGDONG  
Manufacturer Country/AreaChina  
Product Code76EFW  
FDA Product DescriptionTOOTHBRUSH, MANUAL  
Refusal Date10-Nov-2011  
FDA DistrictDET-DO  
Entry/doc/line/sfx 551-9507121-7/1/1
FDA Sample AnalysisNo  
FDA Record of Private Lab Sample Analysis No  
Violation Code Section Charge Statement
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).