JBR, INC.
⚠️ Moderate Risk
FEI: 3015151272 • Sacheon, Gyeongsangnam • SOUTH KOREA
FEI Number
3015151272
Location
Sacheon, Gyeongsangnam
Country
SOUTH KOREAAddress
Jukbangryeomyeongeojohapbeobin, 136 Gusil1-Gil, Sacheon, Gyeongsangnam, South Korea
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
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
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.
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 10/3/2019 | 16AGH01ANCHOVY | 306INSANITARY | Division of West Coast Imports (DWCI) |
| 9/11/2019 | 16AGH01ANCHOVY | 308MFR INSAN | Division of West Coast Imports (DWCI) |
| 8/18/2019 | 16AGH01ANCHOVY | 308MFR INSAN | Division of West Coast Imports (DWCI) |
| 7/2/2019 | 16AGH01ANCHOVY | 308MFR INSAN | Division of West Coast Imports (DWCI) |
Frequently Asked Questions
What is JBR, INC.'s FDA import refusal history?
JBR, INC. (FEI: 3015151272) has 4 FDA import refusal record(s) in our database, spanning from 7/2/2019 to 10/3/2019.
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, INC.'s FEI number is 3015151272.
What types of violations has JBR, INC. received?
JBR, INC. 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 JBR, INC. come from?
All FDA import refusal data for JBR, 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.