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J WELL FRANCE

⚠️ Moderate Risk

FEI: 3012664531 • Paris, Paris • FRANCE

FEI

FEI Number

3012664531

📍

Location

Paris, Paris

🇫🇷

Country

FRANCE
🏢

Address

21 boulevard Ney, , Paris, Paris, France

Moderate Risk

FDA Import Risk Assessment

29.4
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

4
Total Refusals
3
Unique Violations
2/10/2021
Latest Refusal
2/10/2021
Earliest Refusal

Score Breakdown

Violation Severity
43.3×40%
Refusal Volume
25.9×30%
Recency
1.6×20%
Frequency
40.0×10%
How is this score calculated?

Proprietary Algorithm

  • 40% Violation Severity — AI-assessed (1-10)
  • 30% Refusal Volume — Logarithmic scale
  • 20% Recency — Decays over 5 years
  • 10% Frequency — Refusals per year

© ImportRefusal.com Original Analysis

Violation Summary

37814×

TPNOWRNLBL

This article is subject to refusal of admission pursuant to section 801(a)(3) of the FD&C Act in that it is a tobacco product which appears to be misbranded under section 903(a)(8)(B)(i) and 903(a)(1) because its package label does not include a brief statement of the relevant warnings (i.e., one of the four warnings required by section 3 of the Comprehensive Smokeless Tobacco Health Education Act).

38514×

TPLACKFIRM

This article is subject to refusal of admission pursuant to section 801(a)(3) of the Federal Food, Drug, and Cosmetic Act (FD&C Act) because it is a tobacco product in package form that appears to be misbranded under section 903(a)(2)(A) of the FD&C Act in that the label does not contain the name and place of business of the tobacco product manufacturer, packer or distributor.

38544×

TPLKUSSLLB

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act because it is a tobacco product in package form that appears to be misbranded under section 903(a)(2)(D) of the FD&C Act in that the label does not provide the statement "sale only allowed in the United States" and the tobacco product is not subject to any exemptions or variations.

Refusal History

DateProductViolationsDivision
2/10/2021
98LAA02E-CIGARETTE, KIT
3781TPNOWRNLBL
3851TPLACKFIRM
3854TPLKUSSLLB
Division of Southeast Imports (DSEI)
2/10/2021
98MCA01E-LIQUID
3781TPNOWRNLBL
3851TPLACKFIRM
3854TPLKUSSLLB
Division of Southeast Imports (DSEI)
2/10/2021
98MCA01E-LIQUID
3781TPNOWRNLBL
3851TPLACKFIRM
3854TPLKUSSLLB
Division of Southeast Imports (DSEI)
2/10/2021
98MCA01E-LIQUID
3781TPNOWRNLBL
3851TPLACKFIRM
3854TPLKUSSLLB
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is J WELL FRANCE's FDA import refusal history?

J WELL FRANCE (FEI: 3012664531) has 4 FDA import refusal record(s) in our database, spanning from 2/10/2021 to 2/10/2021.

What is an FEI number?

FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. J WELL FRANCE's FEI number is 3012664531.

What types of violations has J WELL FRANCE received?

J WELL FRANCE has been cited for 3 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.

Where does this information about J WELL FRANCE come from?

All FDA import refusal data for J WELL FRANCE is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.

Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.