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AIYA CO LTD

Low Risk

FEI: 1000420902 • Nishio, Aichi • JAPAN

FEI

FEI Number

1000420902

📍

Location

Nishio, Aichi

🇯🇵

Country

JAPAN
🏢

Address

Yokomachiyashiki 15, Kami-Machiyokomachiyas, Nishio, Aichi, Japan

Low Risk

FDA Import Risk Assessment

23.3
LowModerateHighCritical

This firm has a minimal history of FDA import refusals with low-severity violations.

Statistics

3
Total Refusals
3
Unique Violations
12/12/2002
Latest Refusal
10/11/2001
Earliest Refusal

Score Breakdown

Violation Severity
35.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
25.6×10%
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

3202×

LACKS FIRM

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(e)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.

2181×

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.

3281×

USUAL NAME

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)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.

Refusal History

DateProductViolationsDivision
12/12/2002
31KYY02TEA, GREEN
320LACKS FIRM
New Orleans District Office (NOL-DO)
12/12/2002
31KYY02TEA, GREEN
218LIST INGRE
320LACKS FIRM
New Orleans District Office (NOL-DO)
10/11/2001
31KYY99TEA, N.E.C.
328USUAL NAME
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is AIYA CO LTD's FDA import refusal history?

AIYA CO LTD (FEI: 1000420902) has 3 FDA import refusal record(s) in our database, spanning from 10/11/2001 to 12/12/2002.

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. AIYA CO LTD's FEI number is 1000420902.

What types of violations has AIYA CO LTD received?

AIYA CO LTD 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 AIYA CO LTD come from?

All FDA import refusal data for AIYA 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.