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Rejuventum

⚠️ Moderate Risk

FEI: 3011998427 • Ciudad De Mexico, Ciudad de Mexico • MEXICO

FEI

FEI Number

3011998427

📍

Location

Ciudad De Mexico, Ciudad de Mexico

🇲🇽

Country

MEXICO
🏢

Address

Calle Zaragoza 1, Col. Cuajimalpa, Cuajimalpa De Morelos, Ciudad De Mexico, Ciudad de Mexico, Mexico

Moderate Risk

FDA Import Risk Assessment

44.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
2/22/2017
Latest Refusal
2/22/2017
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
Frequency
10.0×10%
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

3101×

POISONOUS

The article is subject to refusal of admission pursuant Section 801(a)(3) in that The cosmetic appears to bear or contain a poisonous or deleterious substance which may render it injurious to users under the conditions prescribed in the labeling thereof, or, under such conditions of use as are customary or usual.

Refusal History

DateProductViolationsDivision
2/22/2017
53LD09SKIN FRESHENERS (SKIN CARE PREPARATIONS)
310POISONOUS
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is Rejuventum's FDA import refusal history?

Rejuventum (FEI: 3011998427) has 1 FDA import refusal record(s) in our database, spanning from 2/22/2017 to 2/22/2017.

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. Rejuventum's FEI number is 3011998427.

What types of violations has Rejuventum received?

Rejuventum has been cited for 1 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 Rejuventum come from?

All FDA import refusal data for Rejuventum 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.