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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 DO7-0097313-7/1/1

Manufacturer FEI3005293463
Manufacturer NameMateur  
Manufacturer Address line 1Bp 1248  
Manufacturer Address line 2  
Manufacturer's CityYaounde  
Manufacturer Province/State  
Manufacturer Country/AreaCameroon  
Product Code61VBL99  
FDA Product DescriptionANTI-FLATULENT N.E.C.  
Refusal Date14-Oct-2005  
FDA DistrictNYK-DO  
Entry/doc/line/sfx DO7-0097313-7/1/1
FDA Sample AnalysisNo  
FDA Record of Private Lab Sample Analysis No  
Violation Code Section Charge Statement
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).  
UNAPPROVED   505(a), 801(a)(3); UNAPPROVED NEW DRUG   The article appears to be a new drug without an approved new drug application.