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Ens

⚠️ Moderate Risk

FEI: 3011067842 • Gyenonggi-do • SOUTH KOREA

FEI

FEI Number

3011067842

📍

Location

Gyenonggi-do

🇰🇷
🏢

Address

501 Hanam Venture Center 239, , Gyenonggi-do, , South Korea

Moderate Risk

FDA Import Risk Assessment

35.0
LowModerateHighCritical

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

Statistics

1
Total Refusals
3
Unique Violations
2/17/2016
Latest Refusal
2/17/2016
Earliest Refusal

Score Breakdown

Violation Severity
76.7×40%
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.

4711×

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.

751×

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
2/17/2016
53LY08PASTE MASKS (MUD PACKS) (SKIN CARE PREPARATIONS)
310POISONOUS
471CSTIC LBLG
75UNAPPROVED
Seattle District Office (SEA-DO)

Frequently Asked Questions

What is Ens's FDA import refusal history?

Ens (FEI: 3011067842) has 1 FDA import refusal record(s) in our database, spanning from 2/17/2016 to 2/17/2016.

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. Ens's FEI number is 3011067842.

What types of violations has Ens received?

Ens has been cited for 3 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 Ens come from?

All FDA import refusal data for Ens 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.