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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 AGL-0020885-1/1/1

Manufacturer FEI3009077329
Manufacturer NameShanghai Zurong Photoelectonic Technology Company  
Manufacturer Address line 1Wuyangdonglu 229hao  
Manufacturer Address line 2  
Manufacturer's CityShanghaishi  
Manufacturer Province/StateShanghaishi  
Manufacturer Country/AreaChina  
Product Code95RFE  
Importer's Product DescriptionLASER ENGRAVE MANCHINE  
Refusal Date07-Nov-2011  
FDA DistrictLOS-DO  
Entry/doc/line/sfx AGL-0020885-1/1/1
FDA Sample AnalysisNo  
FDA Record of Private Lab Sample Analysis No  
Violation Code Section Charge Statement
NO REGISTR   536(a); Failure to file initial report   The article appears to be an electronic product that does not comply with an applicable standard as prescribed by Section 534 because no reporting has been provided as required by Section 537(b).  
NON STD   536(a),(b); NON STANDARD   It appears that the article fails to comply with applicable standards prescribed under section 534.