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SHENZHEN CLEANMO TECHNOLOGY CO L

✅ Low Risk

FEI: 3016701575 • Shenzhen, Guangdong • CHINA

FEI

FEI Number

3016701575

📍

Location

Shenzhen, Guangdong

🇨🇳

Country

CHINA
🏢

Address

Building 103 F Room 608, 22 Qinshengda; Zone, Shenzhen, Guangdong, 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
12/21/2020
Latest Refusal
12/21/2020
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

2231×

FALSE

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose labeling appears to be false or misleading.

3331×

LACKS FIRM

The article is in package form and appears to not bear a label containing the name and place of business of the manufacturer, packer, or distributor.

Refusal History

DateProductViolationsDivision
12/21/2020
80KXFAPPLICATOR, ABSORBENT TIPPED, NON-STERILE
223FALSE
333LACKS FIRM
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is SHENZHEN CLEANMO TECHNOLOGY CO L's FDA import refusal history?

SHENZHEN CLEANMO TECHNOLOGY CO L (FEI: 3016701575) has 1 FDA import refusal record(s) in our database, spanning from 12/21/2020 to 12/21/2020.

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. SHENZHEN CLEANMO TECHNOLOGY CO L's FEI number is 3016701575.

What types of violations has SHENZHEN CLEANMO TECHNOLOGY CO L received?

SHENZHEN CLEANMO TECHNOLOGY CO L 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 SHENZHEN CLEANMO TECHNOLOGY CO L come from?

All FDA import refusal data for SHENZHEN CLEANMO TECHNOLOGY CO L 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.