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SHENZHEN HONGDAO TECHNOLOGY CO L

⚠️ Moderate Risk

FEI: 3025608434 • Hong Kong • HONG KONG

FEI

FEI Number

3025608434

📍

Location

Hong Kong

🇭🇰

Country

HONG KONG
🏢

Address

A 102 No 23 Nanling Rd, , Hong Kong, , Hong Kong

Moderate Risk

FDA Import Risk Assessment

40.1
LowModerateHighCritical

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

Statistics

3
Total Refusals
5
Unique Violations
4/11/2023
Latest Refusal
2/6/2023
Earliest Refusal

Score Breakdown

Violation Severity
61.1×40%
Refusal Volume
22.3×30%
Recency
29.9×20%
Frequency
30.0×10%
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

1182×

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).

24802×

RXPERSONAL

The article appears to be a device which requires a prescription from your doctor.

32802×

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.

5082×

NO 510(K)

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.

841×

RX DEVICE

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a prescription device that appears to not feature a prescription device legend as required by 21 CFR 801.109.

Refusal History

DateProductViolationsDivision
4/11/2023
86MVNLENS, CONTACT (DISPOSABLE)
118NOT LISTED
2480RXPERSONAL
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)
3/9/2023
86LPLLENSES, SOFT CONTACT, DAILY WEAR
84RX DEVICE
Division of Southeast Imports (DSEI)
2/6/2023
86LPLLENSES, SOFT CONTACT, DAILY WEAR
118NOT LISTED
2480RXPERSONAL
3280FRNMFGREG
508NO 510(K)
Division of West Coast Imports (DWCI)

Frequently Asked Questions

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

SHENZHEN HONGDAO TECHNOLOGY CO L (FEI: 3025608434) has 3 FDA import refusal record(s) in our database, spanning from 2/6/2023 to 4/11/2023.

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 HONGDAO TECHNOLOGY CO L's FEI number is 3025608434.

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

SHENZHEN HONGDAO TECHNOLOGY CO L has been cited for 5 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 HONGDAO TECHNOLOGY CO L come from?

All FDA import refusal data for SHENZHEN HONGDAO 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.