• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Import Refusal Report

  • Print
  • Share
  • E-mail
-

Refusal Details as Recorded in OASIS by FDA

for Refusal 112-3405363-0/1/1


Manufacturer FEI3007754401
Manufacturer NameEstafeta Mexicana Sa De Cv  
Manufacturer Address line 1Av Insurgentes No 20barrio De  
Manufacturer Address line 2  
Manufacturer's CityIxmiquilpanixmiquilpan  
Manufacturer Province/State  
Manufacturer Country/AreaMexico  
Product Code53PY99  
Importer's Product Description450392183243 GREEN POWDER SUBSTANCE  
Refusal Date10-Feb-2012  
FDA DistrictNOL-DO  
Entry/doc/line/sfx 112-3405363-0/1/1
FDA Sample AnalysisNo  
FDA Record of Private Lab Sample Analysis No  
Charge(s)
Violation Code Section Charge Statement
LABELING   Section 4(a); 801(a)(3) Misbranding   The article appears in violation of FPLA because of its placement, form and/or contents statement.  
-
-