ImportRefusal LogoImportRefusal

GOPOP HK LIMITED

⚠️ High Risk

FEI: 3027588839 • Dubai • UNITED ARAB EMIRATES

FEI

FEI Number

3027588839

📍

Location

Dubai

🇦🇪
🏢

Address

Rm A1 9f Astoria Bldg34 Ashley, Road Tsim Sha Tsui, Dubai, , United Arab Emirates

High Risk

FDA Import Risk Assessment

56.9
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

8
Total Refusals
4
Unique Violations
11/10/2025
Latest Refusal
8/24/2023
Earliest Refusal

Score Breakdown

Violation Severity
58.5×40%
Refusal Volume
35.3×30%
Recency
96.2×20%
Frequency
36.1×10%
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

32807×

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.

1186×

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).

5084×

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.

2373×

NO PMA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the device appears to be a Class III device and does not appear to have in effect an approved application for premarket approval pursuant to Section 515 of the Act, or an exemption pursuant to Section 520(g)(1).

Refusal History

DateProductViolationsDivision
11/10/2025
86MVNLENS, CONTACT (DISPOSABLE)
237NO PMA
Division of Northeast Imports (DNEI)
10/7/2025
86MVNLENS, CONTACT (DISPOSABLE)
118NOT LISTED
237NO PMA
3280FRNMFGREG
Division of Southeast Imports (DSEI)
10/7/2025
86HQGLENS, SPECTACLE, NON-CUSTOM (PRESCRIPTION)
118NOT LISTED
237NO PMA
3280FRNMFGREG
Division of Southeast Imports (DSEI)
9/26/2025
86HQGLENS, SPECTACLE, NON-CUSTOM (PRESCRIPTION)
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)
9/18/2025
86MVNLENS, CONTACT (DISPOSABLE)
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)
8/13/2025
86MVNLENS, CONTACT (DISPOSABLE)
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)
4/24/2024
86MVNLENS, CONTACT (DISPOSABLE)
3280FRNMFGREG
508NO 510(K)
Division of Northeast Imports (DNEI)
8/24/2023
86MVNLENS, CONTACT (DISPOSABLE)
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is GOPOP HK LIMITED's FDA import refusal history?

GOPOP HK LIMITED (FEI: 3027588839) has 8 FDA import refusal record(s) in our database, spanning from 8/24/2023 to 11/10/2025.

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. GOPOP HK LIMITED's FEI number is 3027588839.

What types of violations has GOPOP HK LIMITED received?

GOPOP HK LIMITED has been cited for 4 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 GOPOP HK LIMITED come from?

All FDA import refusal data for GOPOP HK LIMITED 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.