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Aqualex Co., Ltd.

⚠️ Moderate Risk

FEI: 3010683345 • Seongnam, Gyeonggi • SOUTH KOREA

FEI

FEI Number

3010683345

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Location

Seongnam, Gyeonggi

🇰🇷
🏢

Address

27 Dunchon-Daero 457beon-Gil, Jungwon, 203 Rm, Seongnam, Gyeonggi, South Korea

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
2
Unique Violations
7/16/2024
Latest Refusal
7/16/2024
Earliest Refusal

Score Breakdown

Violation Severity
65.0×40%
Refusal Volume
11.2×30%
Recency
69.9×20%
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

271×

DRUG GMPS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the methods used in and controls used for the manufacture, processing, packing, or holding of drugs and other products do not appear to conform to current good manufacturing practices within the meaning of Section 501(a)(2)(B).

32801×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

Refusal History

DateProductViolationsDivision
7/16/2024
66PBO14OCTINOXATE (ULTRAVIOLET SCREEN/SUNSCREEN)
27DRUG GMPS
3280FRNMFGREG
Division of West Coast Imports (DWCI)

Frequently Asked Questions

What is Aqualex Co., Ltd.'s FDA import refusal history?

Aqualex Co., Ltd. (FEI: 3010683345) has 1 FDA import refusal record(s) in our database, spanning from 7/16/2024 to 7/16/2024.

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. Aqualex Co., Ltd.'s FEI number is 3010683345.

What types of violations has Aqualex Co., Ltd. received?

Aqualex Co., Ltd. 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 Aqualex Co., Ltd. come from?

All FDA import refusal data for Aqualex Co., Ltd. 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.