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JIANGSU DSSHENG RUMBIA BIO-TECH

✅ Low Risk

FEI: 3014303917 • Suzhou • CHINA

FEI

FEI Number

3014303917

📍

Location

Suzhou

🇨🇳

Country

CHINA
🏢

Address

1288 Shexi Road Beishe, , Suzhou, , China

Low Risk

FDA Import Risk Assessment

20.3
LowModerateHighCritical

This firm has a minimal history of FDA import refusals with low-severity violations.

Statistics

1
Total Refusals
2
Unique Violations
5/25/2018
Latest Refusal
5/25/2018
Earliest Refusal

Score Breakdown

Violation Severity
40.0×40%
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

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.

4751×

COSMETLBLG

It appears that the cosmetic consists of two or more ingredients and the label does not list the common or usual name of each ingredient.

Refusal History

DateProductViolationsDivision
5/25/2018
53LY08PASTE MASKS (MUD PACKS) (SKIN CARE PREPARATIONS)
471CSTIC LBLG
475COSMETLBLG
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is JIANGSU DSSHENG RUMBIA BIO-TECH's FDA import refusal history?

JIANGSU DSSHENG RUMBIA BIO-TECH (FEI: 3014303917) has 1 FDA import refusal record(s) in our database, spanning from 5/25/2018 to 5/25/2018.

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. JIANGSU DSSHENG RUMBIA BIO-TECH's FEI number is 3014303917.

What types of violations has JIANGSU DSSHENG RUMBIA BIO-TECH received?

JIANGSU DSSHENG RUMBIA BIO-TECH 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 JIANGSU DSSHENG RUMBIA BIO-TECH come from?

All FDA import refusal data for JIANGSU DSSHENG RUMBIA BIO-TECH 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.