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GENEVA WATCH(HK)COMPANY

⚠️ Moderate Risk

FEI: 3016677137 • Kwai Chung, New Territories • HONG KONG

FEI

FEI Number

3016677137

📍

Location

Kwai Chung, New Territories

🇭🇰

Country

HONG KONG
🏢

Address

10/F, 10/Flat, Metro Loft; 38 Kwai Hei Street, Kwai Chung, New Territories, Hong Kong

Moderate Risk

FDA Import Risk Assessment

32.1
LowModerateHighCritical

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

Statistics

3
Total Refusals
3
Unique Violations
3/3/2022
Latest Refusal
7/29/2020
Earliest Refusal

Score Breakdown

Violation Severity
55.0×40%
Refusal Volume
22.3×30%
Recency
7.7×20%
Frequency
18.8×10%
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

1183×

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).

32803×

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.

Refusal History

DateProductViolationsDivision
3/3/2022
79GAKSUTURE, ABSORBABLE
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Northern Border Imports (DNBI)
8/24/2020
80FLLTHERMOMETER, ELECTRONIC, CLINICAL
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)
7/29/2020
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is GENEVA WATCH(HK)COMPANY's FDA import refusal history?

GENEVA WATCH(HK)COMPANY (FEI: 3016677137) has 3 FDA import refusal record(s) in our database, spanning from 7/29/2020 to 3/3/2022.

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. GENEVA WATCH(HK)COMPANY's FEI number is 3016677137.

What types of violations has GENEVA WATCH(HK)COMPANY received?

GENEVA WATCH(HK)COMPANY 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 GENEVA WATCH(HK)COMPANY come from?

All FDA import refusal data for GENEVA WATCH(HK)COMPANY 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.