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ASADA CO.,LTD.

⚠️ Moderate Risk

FEI: 3004278243 • Nagoya, Aichi • JAPAN

FEI

FEI Number

3004278243

📍

Location

Nagoya, Aichi

🇯🇵

Country

JAPAN
🏢

Address

181 Aiti, Inanishi-Cho; Nakamura, Nagoya, Aichi, Japan

Moderate Risk

FDA Import Risk Assessment

26.7
LowModerateHighCritical

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

Statistics

1
Total Refusals
5
Unique Violations
12/29/2016
Latest Refusal
12/29/2016
Earliest Refusal

Score Breakdown

Violation Severity
56.0×40%
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

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.

4731×

LABELING

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

4821×

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.

621×

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).

831×

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.

Refusal History

DateProductViolationsDivision
12/29/2016
24TGT03BAMBOO SHOOTS (LEAF & STEM VEGETABLE)
218LIST INGRE
473LABELING
482NUTRIT LBL
62NEEDS FCE
83NO PROCESS
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is ASADA CO.,LTD.'s FDA import refusal history?

ASADA CO.,LTD. (FEI: 3004278243) has 1 FDA import refusal record(s) in our database, spanning from 12/29/2016 to 12/29/2016.

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. ASADA CO.,LTD.'s FEI number is 3004278243.

What types of violations has ASADA CO.,LTD. received?

ASADA CO.,LTD. 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 ASADA CO.,LTD. come from?

All FDA import refusal data for ASADA 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.