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Johnson & Johnson (Hk) Ltd - Finance

⚠️ Moderate Risk

FEI: 3003271546 • Mong Kok, Kowloon • HONG KONG

FEI

FEI Number

3003271546

📍

Location

Mong Kok, Kowloon

🇭🇰

Country

HONG KONG
🏢

Address

13/G, Grand Century Place, Mong Kok, Kowloon, Hong Kong

Moderate Risk

FDA Import Risk Assessment

25.9
LowModerateHighCritical

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

Statistics

1
Total Refusals
5
Unique Violations
6/23/2016
Latest Refusal
6/23/2016
Earliest Refusal

Score Breakdown

Violation Severity
54.0×40%
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

1181×

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).

32601×

NO ENGLISH

Required label or labeling appears to not be in English in violation of 21 C.F.R. 801.15(c)(1)

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.

5081×

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
6/23/2016
86LPLLENSES, SOFT CONTACT, DAILY WEAR
118NOT LISTED
3260NO ENGLISH
3280FRNMFGREG
508NO 510(K)
84RX DEVICE
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is Johnson & Johnson (Hk) Ltd - Finance's FDA import refusal history?

Johnson & Johnson (Hk) Ltd - Finance (FEI: 3003271546) has 1 FDA import refusal record(s) in our database, spanning from 6/23/2016 to 6/23/2016.

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. Johnson & Johnson (Hk) Ltd - Finance's FEI number is 3003271546.

What types of violations has Johnson & Johnson (Hk) Ltd - Finance received?

Johnson & Johnson (Hk) Ltd - Finance 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 Johnson & Johnson (Hk) Ltd - Finance come from?

All FDA import refusal data for Johnson & Johnson (Hk) Ltd - Finance 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.