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LABORATOIRES BAILLEUL

⚠️ Moderate Risk

FEI: 3015320615 • Luxemburg • LUXEMBOURG

FEI

FEI Number

3015320615

📍

Location

Luxemburg

🇱🇺

Country

LUXEMBOURG
🏢

Address

10 Avenue Pasteur, , Luxemburg, , Luxembourg

Moderate Risk

FDA Import Risk Assessment

42.9
LowModerateHighCritical

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

Statistics

2
Total Refusals
4
Unique Violations
1/27/2025
Latest Refusal
11/13/2019
Earliest Refusal

Score Breakdown

Violation Severity
52.5×40%
Refusal Volume
17.7×30%
Recency
80.9×20%
Frequency
3.8×10%
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

23001×

DIETARYLBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it is a dietary supplement that appears to be misbranded within the meaning of Section 403(s)(2)(B) of the FD&C Act in that the label or labeling fails to identify the product by using the term "dietary supplement", which term may be modified with the name of such an ingredient.

38641×

NCONTACT

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it is a dietary supplement that appears to be misbranded within the meaning of Section 403(y) of the FD&C Act in that the dietary supplement label fails to bear a domestic address or phone number through which the responsible person (as described in section 761 of the FD&C Act) may receive a report of a serious adverse event with such dietary supplement.

4821×

NUTRIT LBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.

751×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

Refusal History

DateProductViolationsDivision
1/27/2025
64XCE07TRETINOIN (KERATOLYTIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)
11/13/2019
54YYY99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
2300DIETARYLBL
3864NCONTACT
482NUTRIT LBL
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is LABORATOIRES BAILLEUL's FDA import refusal history?

LABORATOIRES BAILLEUL (FEI: 3015320615) has 2 FDA import refusal record(s) in our database, spanning from 11/13/2019 to 1/27/2025.

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. LABORATOIRES BAILLEUL's FEI number is 3015320615.

What types of violations has LABORATOIRES BAILLEUL received?

LABORATOIRES BAILLEUL has been cited for 4 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 LABORATOIRES BAILLEUL come from?

All FDA import refusal data for LABORATOIRES BAILLEUL 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.