• 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 112-8601643-5/1/1/A


Manufacturer FEI3004333939
Manufacturer NameNSE Products  
Manufacturer Address line 11325 S 275 E  
Manufacturer Address line 2  
Manufacturer's CityProvo  
Manufacturer Province/StateUT  
Manufacturer Country/AreaUnited States  
Product Code89NZF  
FDA Product DescriptionMASSAGER, COSMETIC, STATIC ELECTRICITY-EMITTING  
Refusal Date15-Sep-2010  
FDA DistrictFLA-DO  
Entry/doc/line/sfx 112-8601643-5/1/1/A
FDA Sample AnalysisNo  
FDA Record of Private Lab Sample Analysis No  
Charge(s)
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).  
REGISTERED   502(o), 801(a)(3); MISBRANDING   It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).  
-
-