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COOMEX SOURCES CO LTD

⚠️ Moderate Risk

FEI: 3012353272 • Qingdao, Shandong • CHINA

FEI

FEI Number

3012353272

📍

Location

Qingdao, Shandong

🇨🇳

Country

CHINA
🏢

Address

Xiwang Tower Room 903, # 138 Dunhualu, Qingdao, Shandong, China

Moderate Risk

FDA Import Risk Assessment

34.8
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
8/26/2024
Latest Refusal
8/26/2024
Earliest Refusal

Score Breakdown

Violation Severity
40.0×40%
Refusal Volume
11.2×30%
Recency
72.1×20%
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

1181×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

3411×

REGISTERED

It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).

Refusal History

DateProductViolationsDivision
8/26/2024
80KCTSTERILIZATION WRAP CONTAINERS, TRAYS, CASSETTES & OTHER ACCESSORIES
118NOT LISTED
341REGISTERED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is COOMEX SOURCES CO LTD's FDA import refusal history?

COOMEX SOURCES CO LTD (FEI: 3012353272) has 1 FDA import refusal record(s) in our database, spanning from 8/26/2024 to 8/26/2024.

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. COOMEX SOURCES CO LTD's FEI number is 3012353272.

What types of violations has COOMEX SOURCES CO LTD received?

COOMEX SOURCES CO LTD 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 COOMEX SOURCES CO LTD come from?

All FDA import refusal data for COOMEX SOURCES CO LTD 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.