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JRS CORP

⚠️ Moderate Risk

FEI: 3015530871 • Aichi Ken • JAPAN

FEI

FEI Number

3015530871

📍

Location

Aichi Ken

🇯🇵

Country

JAPAN
🏢

Address

Nisiazima1-701, Nishiaj, , Aichi Ken, , Japan

Moderate Risk

FDA Import Risk Assessment

25.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
9/3/2019
Latest Refusal
9/3/2019
Earliest Refusal

Score Breakdown

Violation Severity
40.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
30.0×10%
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

4733×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

Refusal History

DateProductViolationsDivision
9/3/2019
53LD01CLEANSING (COLD CREAMS, CLEANSING LOTIONS, LIQUIDS, PADS) (SKIN CARE PREPARATIONS)
473LABELING
Division of Southeast Imports (DSEI)
9/3/2019
53LD01CLEANSING (COLD CREAMS, CLEANSING LOTIONS, LIQUIDS, PADS) (SKIN CARE PREPARATIONS)
473LABELING
Division of Southeast Imports (DSEI)
9/3/2019
53LD01CLEANSING (COLD CREAMS, CLEANSING LOTIONS, LIQUIDS, PADS) (SKIN CARE PREPARATIONS)
473LABELING
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is JRS CORP's FDA import refusal history?

JRS CORP (FEI: 3015530871) has 3 FDA import refusal record(s) in our database, spanning from 9/3/2019 to 9/3/2019.

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. JRS CORP's FEI number is 3015530871.

What types of violations has JRS CORP received?

JRS CORP 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 JRS CORP come from?

All FDA import refusal data for JRS CORP 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.