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Mosbeau Co Ltd

⚠️ Moderate Risk

FEI: 3010250175 • Ashiya-shi, Hyogo-ken • JAPAN

FEI

FEI Number

3010250175

📍

Location

Ashiya-shi, Hyogo-ken

🇯🇵

Country

JAPAN
🏢

Address

2-21 Chayano-Cho Ashiya-Shi May Peace, , Ashiya-shi, Hyogo-ken, Japan

Moderate Risk

FDA Import Risk Assessment

33.1
LowModerateHighCritical

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

Statistics

3
Total Refusals
4
Unique Violations
7/8/2013
Latest Refusal
7/8/2013
Earliest Refusal

Score Breakdown

Violation Severity
58.6×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
30.0×10%
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

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).

752×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

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.

37411×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(o) in that it is being imported or offered for import into the United States, and the importer, owner, or consignee of such article did not, at the time of offering the article for import, submit to the Secretary a statement that identifies the registration under section 510(i) of the Act of each establishment that with respect to such article is required under such section to register with the Secretary.

Refusal History

DateProductViolationsDivision
7/8/2013
53LD06MOISTURIZING (SKIN CARE PREPARATIONS)
118NOT LISTED
3741FRNMFGREG
75UNAPPROVED
Cincinnati District Office (CIN-DO)
7/8/2013
63VDJ99DEPIGMENTOR N.E.C.
118NOT LISTED
3280FRNMFGREG
75UNAPPROVED
Cincinnati District Office (CIN-DO)
7/8/2013
53LC06MOISTURIZING (SKIN CARE PREPARATIONS)
118NOT LISTED
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is Mosbeau Co Ltd's FDA import refusal history?

Mosbeau Co Ltd (FEI: 3010250175) has 3 FDA import refusal record(s) in our database, spanning from 7/8/2013 to 7/8/2013.

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. Mosbeau Co Ltd's FEI number is 3010250175.

What types of violations has Mosbeau Co Ltd received?

Mosbeau Co Ltd 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 Mosbeau Co Ltd come from?

All FDA import refusal data for Mosbeau 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.