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Fuji Latex Co., Ltd.

⚠️ Moderate Risk

FEI: 2855 • Chiyoda, Tokyo • JAPAN

FEI

FEI Number

2855

📍

Location

Chiyoda, Tokyo

🇯🇵

Country

JAPAN
🏢

Address

, 3-Chome, Kanda Nishiki-Cho, 19 1, Chiyoda, Tokyo, Japan

Moderate Risk

FDA Import Risk Assessment

34.5
LowModerateHighCritical

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

Statistics

6
Total Refusals
6
Unique Violations
7/28/2017
Latest Refusal
3/21/2017
Earliest Refusal

Score Breakdown

Violation Severity
47.9×40%
Refusal Volume
31.3×30%
Recency
0.0×20%
Frequency
60.0×10%
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

32605×

NO ENGLISH

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

1184×

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.

162×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

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.

3332×

LACKS FIRM

The article is in package form and appears to not bear a label containing the name and place of business of the manufacturer, packer, or distributor.

Refusal History

DateProductViolationsDivision
7/28/2017
85HISCONDOM
118NOT LISTED
3260NO ENGLISH
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)
7/28/2017
85HISCONDOM
118NOT LISTED
3260NO ENGLISH
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)
7/28/2017
85HISCONDOM
16DIRECTIONS
3260NO ENGLISH
333LACKS FIRM
Division of Southeast Imports (DSEI)
7/28/2017
85HISCONDOM
16DIRECTIONS
333LACKS FIRM
Division of Southeast Imports (DSEI)
5/26/2017
85HISCONDOM
118NOT LISTED
3260NO ENGLISH
508NO 510(K)
Division of Southeast Imports (DSEI)
3/21/2017
85HISCONDOM
118NOT LISTED
3260NO ENGLISH
508NO 510(K)
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Fuji Latex Co., Ltd.'s FDA import refusal history?

Fuji Latex Co., Ltd. (FEI: 2855) has 6 FDA import refusal record(s) in our database, spanning from 3/21/2017 to 7/28/2017.

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. Fuji Latex Co., Ltd.'s FEI number is 2855.

What types of violations has Fuji Latex Co., Ltd. received?

Fuji Latex Co., Ltd. has been cited for 6 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 Fuji Latex Co., Ltd. come from?

All FDA import refusal data for Fuji Latex Co., Ltd. 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.