• 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 WX6-0015803-3/14/1

Manufacturer FEI3004271362
Manufacturer Name"Biona-plus" Ltd  
Manufacturer Address line 19, Tsiolkovskogo street  
Manufacturer Address line 2  
Manufacturer's CityChernigov  
Manufacturer Province/StateUA-74  
Manufacturer Country/AreaUkraine  
Product Code24FCY20  
Refusal Date25-Jan-2005  
FDA DistrictSAN-DO  
Entry/doc/line/sfx WX6-0015803-3/14/1
FDA Sample AnalysisNo  
FDA Record of Private Lab Sample Analysis No  
Violation Code Section Charge Statement
NEEDS FCE   402(a)(4), 801(a)(3); ADULTERATION   It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).  
NO PROCESS   402(a)(4), 801(a)(3); ADULTERATION   The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.