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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 315-7124539-3/1/1


Manufacturer FEI3001124005
Manufacturer NameBrimar Ltd.  
Manufacturer Address line 1Greenside Way  
Manufacturer Address line 2  
Manufacturer's CityManchester  
Manufacturer Province/State  
Manufacturer Country/AreaUnited Kingdom  
Product Code94V05  
Importer's Product DescriptionCATHODE RAY TUBE  
Refusal Date07-May-2002  
FDA DistrictNYK-DO  
Entry/doc/line/sfx 315-7124539-3/1/1
FDA Sample AnalysisNo  
FDA Record of Private Lab Sample Analysis No  
Charge(s)
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).  
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