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Benton Inc.

⚠️ Moderate Risk

FEI: 3011883357 • Dongjak District, Seoul • SOUTH KOREA

FEI

FEI Number

3011883357

📍

Location

Dongjak District, Seoul

🇰🇷
🏢

Address

8 Yeouidaebang-Ro 24sa-Gil, , Dongjak District, Seoul, South Korea

Moderate Risk

FDA Import Risk Assessment

49.9
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
5/8/2023
Latest Refusal
3/2/2020
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
22.3×30%
Recency
31.3×20%
Frequency
9.4×10%
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

753×

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
5/8/2023
53LD99OTHER SKIN CARE PREPARATIONS, N.E.C.
75UNAPPROVED
Division of Southeast Imports (DSEI)
3/2/2020
53LD03FACE,BODY,AND HAND (EXCLUDING SHAVING PREPARATIONS) (SKIN CARE PREPARATIONS)
75UNAPPROVED
Division of Northern Border Imports (DNBI)
3/2/2020
53LD99OTHER SKIN CARE PREPARATIONS, N.E.C.
75UNAPPROVED
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is Benton Inc.'s FDA import refusal history?

Benton Inc. (FEI: 3011883357) has 3 FDA import refusal record(s) in our database, spanning from 3/2/2020 to 5/8/2023.

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. Benton Inc.'s FEI number is 3011883357.

What types of violations has Benton Inc. received?

Benton Inc. 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 Benton Inc. come from?

All FDA import refusal data for Benton Inc. 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.