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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 AEK-8796889-3/1/1

Manufacturer FEI3009027407
Manufacturer NameForever Beauty Laser Co., Ltd  
Manufacturer Address line 1702-1-11 NO2 Jiuzhouxiya Xizonglv Chang  
Manufacturer Address line 2Fang Shan District  
Manufacturer's CityBeijing  
Manufacturer Province/State  
Manufacturer Country/AreaChina  
Product Code79NUV  
Refusal Date25-Nov-2011  
FDA DistrictCIN-DO  
Entry/doc/line/sfx AEK-8796889-3/1/1
FDA Sample AnalysisNo  
FDA Record of Private Lab Sample Analysis No  
Violation Code Section Charge Statement
DIRECTIONS   502(f)(1), 801(a)(3); MISBRANDING   The article appears to lack adequate directions for use.  
NO 510(K)   801(a)(3); 502(o) Misbranding   It appears that a notice or other information respecting the device was not provided to FDA, as required by Section 510(k) and the device was not found to be substantially equivalent to a predicate device.  
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).