ImportRefusal LogoImportRefusal

Rejuvenal Europe BV

⚠️ Moderate Risk

FEI: 2000021273 • Buchten, Limburg • NETHERLANDS

FEI

FEI Number

2000021273

📍

Location

Buchten, Limburg

🇳🇱
🏢

Address

Dorpstraat 74, , Buchten, Limburg, Netherlands

Moderate Risk

FDA Import Risk Assessment

25.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
2
Unique Violations
6/20/2007
Latest Refusal
6/20/2007
Earliest Refusal

Score Breakdown

Violation Severity
40.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
30.0×10%
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

4713×

CSTIC LBLG

The labeling appears to fail to comply with cosmetic labeling requirements of Section 602(a), and/or (b), and/or (c), and as identified by 21 C.F.R. Part 701.

4751×

COSMETLBLG

It appears that the cosmetic consists of two or more ingredients and the label does not list the common or usual name of each ingredient.

Refusal History

DateProductViolationsDivision
6/20/2007
53LC99OTHER SKIN CARE PREPARATIONS, N.E.C.
471CSTIC LBLG
475COSMETLBLG
New Orleans District Office (NOL-DO)
6/20/2007
53LD99OTHER SKIN CARE PREPARATIONS, N.E.C.
471CSTIC LBLG
New Orleans District Office (NOL-DO)
6/20/2007
53LY99OTHER SKIN CARE PREPARATIONS, N.E.C.
471CSTIC LBLG
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Rejuvenal Europe BV's FDA import refusal history?

Rejuvenal Europe BV (FEI: 2000021273) has 3 FDA import refusal record(s) in our database, spanning from 6/20/2007 to 6/20/2007.

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. Rejuvenal Europe BV's FEI number is 2000021273.

What types of violations has Rejuvenal Europe BV received?

Rejuvenal Europe BV has been cited for 2 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 Rejuvenal Europe BV come from?

All FDA import refusal data for Rejuvenal Europe BV 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.