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Shenzhen Fullair Co

✅ Low Risk

FEI: 3011144938 • Nanshan • HONG KONG

FEI

FEI Number

3011144938

📍

Location

Nanshan

🇭🇰

Country

HONG KONG
🏢

Address

No 2 Duchen Gong Zhongshan, , Nanshan, , Hong Kong

Low Risk

FDA Import Risk Assessment

24.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
3
Unique Violations
12/12/2014
Latest Refusal
12/12/2014
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
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

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.

4741×

COSMETLBLG

It appears the label does not bear the common or usual name of the cosmetic.

751×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

Refusal History

DateProductViolationsDivision
12/12/2014
53LC06MOISTURIZING (SKIN CARE PREPARATIONS)
333LACKS FIRM
474COSMETLBLG
75UNAPPROVED
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Shenzhen Fullair Co's FDA import refusal history?

Shenzhen Fullair Co (FEI: 3011144938) has 1 FDA import refusal record(s) in our database, spanning from 12/12/2014 to 12/12/2014.

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 Fullair Co's FEI number is 3011144938.

What types of violations has Shenzhen Fullair Co received?

Shenzhen Fullair Co has been cited for 3 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 Fullair Co come from?

All FDA import refusal data for Shenzhen Fullair Co 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.