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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 EJ2-0101704-6/1/1

Manufacturer FEI3010441353
Manufacturer NameGUANGDONG CANNERY  
Manufacturer Address line 1NO. 15 INDUSTRY AVENUE, CONGHUA  
Manufacturer Address line 2DEVELOPMENT ZONE  
Manufacturer's CityGuangzhou City  
Manufacturer Province/StateYandongsheng  
Manufacturer Country/AreaChina  
Product Code16AEE57  
FDA Product DescriptionDACE  
Refusal Date09-Nov-2011  
FDA DistrictLOS-DO  
Entry/doc/line/sfx EJ2-0101704-6/1/1
FDA Sample AnalysisNo  
FDA Record of Private Lab Sample Analysis Yes  
Violation Code Section Charge Statement
UNSAFE ADD   402(a)(2)(C)(i), 801(a)(3); ADULTERATION   The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be adulterated because it appears to contain a poisonous or deleterious substance which may render it injurious to health [Adulteration, Section 402(a)(1)].  
VETDRUGRES   402(a)(2)(C)(ii); 801(a)(3); ADULTERATION   The article appears to contain a new animal drug (or conversion product thereof) that is unsafe within the meaning of section 512. Product contains