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KUBO OPTICAL PRODUCTS

⚠️ Moderate Risk

FEI: 3034208374 • Shanghai • CHINA

FEI

FEI Number

3034208374

📍

Location

Shanghai

🇨🇳

Country

CHINA
🏢

Address

Rm 15f03-06a No 1111 Ch, , Shanghai, , China

Moderate Risk

FDA Import Risk Assessment

40.5
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
1/30/2025
Latest Refusal
1/30/2025
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
Refusal Volume
11.2×30%
Recency
80.8×20%
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

32801×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

Refusal History

DateProductViolationsDivision
1/30/2025
86LPLLENSES, SOFT CONTACT, DAILY WEAR
3280FRNMFGREG
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is KUBO OPTICAL PRODUCTS's FDA import refusal history?

KUBO OPTICAL PRODUCTS (FEI: 3034208374) has 1 FDA import refusal record(s) in our database, spanning from 1/30/2025 to 1/30/2025.

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. KUBO OPTICAL PRODUCTS's FEI number is 3034208374.

What types of violations has KUBO OPTICAL PRODUCTS received?

KUBO OPTICAL PRODUCTS 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 KUBO OPTICAL PRODUCTS come from?

All FDA import refusal data for KUBO OPTICAL PRODUCTS 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.