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ASADA CO.,LTD.

⚠️ Moderate Risk

FEI: 3005057847 • Nagoya, Aichi • JAPAN

FEI

FEI Number

3005057847

📍

Location

Nagoya, Aichi

🇯🇵

Country

JAPAN
🏢

Address

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

Moderate Risk

FDA Import Risk Assessment

30.5
LowModerateHighCritical

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

Statistics

3
Total Refusals
4
Unique Violations
4/6/2009
Latest Refusal
2/18/2003
Earliest Refusal

Score Breakdown

Violation Severity
58.3×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
4.9×10%
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

3212×

LACKS N/C

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)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.

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.

111×

UNSAFE COL

The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).

4731×

LABELING

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

Refusal History

DateProductViolationsDivision
4/6/2009
25JCT24GINGER ROOT (ROOT & TUBER VEGETABLE)
11UNSAFE COL
New York District Office (NYK-DO)
2/18/2003
25JGT24GINGER ROOT (ROOT & TUBER VEGETABLE)
321LACKS N/C
473LABELING
83NO PROCESS
Los Angeles District Office (LOS-DO)
2/18/2003
25JCT24GINGER ROOT (ROOT & TUBER VEGETABLE)
321LACKS N/C
83NO PROCESS
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

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

ASADA CO.,LTD. (FEI: 3005057847) has 3 FDA import refusal record(s) in our database, spanning from 2/18/2003 to 4/6/2009.

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 3005057847.

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

ASADA 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 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.