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Maesa

⚠️ Moderate Risk

FEI: 3008464161 • Zhuhai, Guangdong • CHINA

FEI

FEI Number

3008464161

📍

Location

Zhuhai, Guangdong

🇨🇳

Country

CHINA
🏢

Address

Zhuhai Avenue Jin Wan Xincun, , Zhuhai, Guangdong, China

Moderate Risk

FDA Import Risk Assessment

49.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
11/29/2010
Latest Refusal
11/29/2010
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
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

3103×

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
11/29/2010
53GD05LIPSTICK (MAKEUP PREPARATIONS, NOT FOR EYES)
310POISONOUS
New York District Office (NYK-DO)
11/29/2010
53GD05LIPSTICK (MAKEUP PREPARATIONS, NOT FOR EYES)
310POISONOUS
New York District Office (NYK-DO)
11/29/2010
53GK05LIPSTICK (MAKEUP PREPARATIONS, NOT FOR EYES)
310POISONOUS
New York District Office (NYK-DO)

Frequently Asked Questions

What is Maesa's FDA import refusal history?

Maesa (FEI: 3008464161) has 3 FDA import refusal record(s) in our database, spanning from 11/29/2010 to 11/29/2010.

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. Maesa's FEI number is 3008464161.

What types of violations has Maesa received?

Maesa 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 Maesa come from?

All FDA import refusal data for Maesa 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.