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Fancl Corporation

⚠️ High Risk

FEI: 3000192030 • Kanagawa, Kanagawa • JAPAN

FEI

FEI Number

3000192030

📍

Location

Kanagawa, Kanagawa

🇯🇵

Country

JAPAN
🏢

Address

109-1 Iijima-Cho, Sakae-Ku, , Yokohama, Kanagawa, Kanagawa, Japan

High Risk

FDA Import Risk Assessment

50.3
LowModerateHighCritical

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

Statistics

26
Total Refusals
12
Unique Violations
12/15/2004
Latest Refusal
12/17/2001
Earliest Refusal

Score Breakdown

Violation Severity
64.4×40%
Refusal Volume
53.0×30%
Recency
0.0×20%
Frequency
86.8×10%
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

31314×

HELD INSAN

The cosmetic appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.

3245×

NO ENGLISH

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).

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).

4883×

HEALTH C

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling bears an unauthorized nutrient content/health claim.

2183×

LIST INGRE

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.

832×

NO PROCESS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.

4822×

NUTRIT LBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.

622×

NEEDS FCE

It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).

3081×

MFR INSAN

The article is subject to refusal of admission pursuant to section 801(a)(1) in that the article appears to have been manufactured, processed, or packed under insanitary conditions.

4721×

NO ENGLISH

Required label or labeling appears to not be in English in violation of 21 C.F.R. 201.15(c)(1).

4731×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

4751×

COSMETLBLG

It appears that the cosmetic consists of two or more ingredients and the label does not list the common or usual name of each ingredient.

Refusal History

DateProductViolationsDivision
12/15/2004
66PBJ99ULTRAVIOLET SCREEN/SUNSCREEN N.E.C.
118NOT LISTED
Los Angeles District Office (LOS-DO)
9/18/2004
53LC07NIGHT (SKIN CARE PREPARATIONS)
475COSMETLBLG
Los Angeles District Office (LOS-DO)
9/18/2004
66VAJ99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
Los Angeles District Office (LOS-DO)
6/8/2004
66PBJ99ULTRAVIOLET SCREEN/SUNSCREEN N.E.C.
118NOT LISTED
Los Angeles District Office (LOS-DO)
6/8/2004
66PBJ99ULTRAVIOLET SCREEN/SUNSCREEN N.E.C.
118NOT LISTED
Los Angeles District Office (LOS-DO)
6/1/2004
53LC07NIGHT (SKIN CARE PREPARATIONS)
473LABELING
Los Angeles District Office (LOS-DO)
3/9/2003
54FCC99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
218LIST INGRE
324NO ENGLISH
472NO ENGLISH
488HEALTH C
Los Angeles District Office (LOS-DO)
9/4/2002
54FCC99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
218LIST INGRE
324NO ENGLISH
488HEALTH C
Los Angeles District Office (LOS-DO)
9/4/2002
54FCC99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
218LIST INGRE
324NO ENGLISH
488HEALTH C
Los Angeles District Office (LOS-DO)
5/22/2002
02AHE05RICE, CULTIVATED, WHOLE GRAIN
324NO ENGLISH
482NUTRIT LBL
62NEEDS FCE
83NO PROCESS
Los Angeles District Office (LOS-DO)
5/22/2002
02AHE05RICE, CULTIVATED, WHOLE GRAIN
324NO ENGLISH
482NUTRIT LBL
62NEEDS FCE
83NO PROCESS
Los Angeles District Office (LOS-DO)
1/3/2002
53GK05LIPSTICK (MAKEUP PREPARATIONS, NOT FOR EYES)
313HELD INSAN
Los Angeles District Office (LOS-DO)
1/3/2002
53GK05LIPSTICK (MAKEUP PREPARATIONS, NOT FOR EYES)
313HELD INSAN
Los Angeles District Office (LOS-DO)
1/3/2002
53GK05LIPSTICK (MAKEUP PREPARATIONS, NOT FOR EYES)
313HELD INSAN
Los Angeles District Office (LOS-DO)
1/3/2002
53CK01EYEBROW PENCIL (EYE MAKEUP PREPARATIONS)
313HELD INSAN
Los Angeles District Office (LOS-DO)
1/3/2002
53CK01EYEBROW PENCIL (EYE MAKEUP PREPARATIONS)
313HELD INSAN
Los Angeles District Office (LOS-DO)
1/3/2002
53GH02FACE POWDERS (MAKEUP PREPARATIONS, NOT FOR EYES)
313HELD INSAN
Los Angeles District Office (LOS-DO)
1/3/2002
53GH03FOUNDATIONS (MAKEUP PREPARATIONS, NOT FOR EYES)
313HELD INSAN
Los Angeles District Office (LOS-DO)
1/3/2002
53GH03FOUNDATIONS (MAKEUP PREPARATIONS, NOT FOR EYES)
313HELD INSAN
Los Angeles District Office (LOS-DO)
1/3/2002
53GH03FOUNDATIONS (MAKEUP PREPARATIONS, NOT FOR EYES)
313HELD INSAN
Los Angeles District Office (LOS-DO)
1/3/2002
53GC03FOUNDATIONS (MAKEUP PREPARATIONS, NOT FOR EYES)
313HELD INSAN
Los Angeles District Office (LOS-DO)
1/3/2002
53GC03FOUNDATIONS (MAKEUP PREPARATIONS, NOT FOR EYES)
313HELD INSAN
Los Angeles District Office (LOS-DO)
1/3/2002
53GD03FOUNDATIONS (MAKEUP PREPARATIONS, NOT FOR EYES)
313HELD INSAN
Los Angeles District Office (LOS-DO)
1/3/2002
53LD06MOISTURIZING (SKIN CARE PREPARATIONS)
313HELD INSAN
Los Angeles District Office (LOS-DO)
1/3/2002
53GD03FOUNDATIONS (MAKEUP PREPARATIONS, NOT FOR EYES)
313HELD INSAN
Los Angeles District Office (LOS-DO)
12/17/2001
54FCL99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
308MFR INSAN
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Fancl Corporation's FDA import refusal history?

Fancl Corporation (FEI: 3000192030) has 26 FDA import refusal record(s) in our database, spanning from 12/17/2001 to 12/15/2004.

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. Fancl Corporation's FEI number is 3000192030.

What types of violations has Fancl Corporation received?

Fancl Corporation has been cited for 12 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 Fancl Corporation come from?

All FDA import refusal data for Fancl Corporation 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.