ImportRefusal LogoImportRefusal

JBR

⚠️ High Risk

FEI: 3029914863 • Tongyeong, Gyeongsangnam • SOUTH KOREA

FEI

FEI Number

3029914863

📍

Location

Tongyeong, Gyeongsangnam

🇰🇷
🏢

Address

2119 Dosanilju-Ro, Dosan-Myeon, Tongyeong, Gyeongsangnam, South Korea

High Risk

FDA Import Risk Assessment

72.1
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

8
Total Refusals
5
Unique Violations
11/4/2025
Latest Refusal
8/19/2024
Earliest Refusal

Score Breakdown

Violation Severity
89.0×40%
Refusal Volume
35.3×30%
Recency
96.3×20%
Frequency
66.1×10%
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

2518×

POISONOUS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a poisonous or deleterious substance which may render the article injurious to health. Contains:

3068×

INSANITARY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.

3082×

MFR INSAN

The article is subject to refusal of admission pursuant to section 801(a)(1) in that the article appears to have been manufactured, processed, or packed under insanitary conditions.

2561×

INCONSPICU

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).

2601×

FALSE

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.

Refusal History

DateProductViolationsDivision
11/4/2025
16EGD03OYSTERS
251POISONOUS
306INSANITARY
Division of Northern Border Imports (DNBI)
11/4/2025
16EGD03OYSTERS
251POISONOUS
306INSANITARY
Division of Northern Border Imports (DNBI)
10/2/2025
16EGD03OYSTERS
251POISONOUS
306INSANITARY
Division of West Coast Imports (DWCI)
10/2/2025
16EGD03OYSTERS
251POISONOUS
306INSANITARY
Division of West Coast Imports (DWCI)
10/2/2025
16EGD03OYSTERS
251POISONOUS
306INSANITARY
Division of West Coast Imports (DWCI)
9/16/2025
16EGD03OYSTERS
251POISONOUS
306INSANITARY
308MFR INSAN
Division of West Coast Imports (DWCI)
9/16/2025
16EGD03OYSTERS
251POISONOUS
306INSANITARY
308MFR INSAN
Division of West Coast Imports (DWCI)
8/19/2024
16XGT32OYSTERS, AQUACULTURE HARVESTED FISHERY/SEAFOOD PRODUCTS
251POISONOUS
256INCONSPICU
260FALSE
306INSANITARY
Division of West Coast Imports (DWCI)

Frequently Asked Questions

What is JBR's FDA import refusal history?

JBR (FEI: 3029914863) has 8 FDA import refusal record(s) in our database, spanning from 8/19/2024 to 11/4/2025.

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. JBR's FEI number is 3029914863.

What types of violations has JBR received?

JBR has been cited for 5 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 JBR come from?

All FDA import refusal data for JBR 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.