new honda international inc.
⚠️ Moderate Risk
FEI: 3013288920 • Wuchi District, TW-TXQ • TAIWAN
FEI Number
3013288920
Location
Wuchi District, TW-TXQ
Country
TAIWANAddress
No.114,Syh-Wai West Road, , Wuchi District, TW-TXQ, Taiwan
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
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
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).
SULFITELBL
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded because 1) it appears to contain sulfites but the label fails to declare the presence of sulfites, a fact material to sulfite-sensitive individuals who must avoid the ingredient due to potential health consequences from its consumption, and 2) it appears the food is fabricated from two or more ingredients and the label does not list the common or usual name of each ingredient.
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).
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.
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 6/7/2011 | 24TVI03BAMBOO SHOOTS (LEAF & STEM VEGETABLE) | New York District Office (NYK-DO) | |
| 3/15/2011 | 24VGE03BAMBOO SHOOTS, WITH SAUCE | 2040SULFITELBL | New York District Office (NYK-DO) |
| 3/15/2011 | 24VGE12CHINESE CABBAGE, WITH SAUCE | 218LIST INGRE | New York District Office (NYK-DO) |
| 7/19/2007 | 24TGE03BAMBOO SHOOTS (LEAF & STEM VEGETABLE) | Los Angeles District Office (LOS-DO) | |
| 1/24/2006 | 21TGH18LONGAN, DRIED OR PASTE | 11UNSAFE COL | New York District Office (NYK-DO) |
| 1/24/2006 | 21TGH19LYCHEE, LICHEE, LITCHI, LEECHEE, DRIED OR PASTE | 11UNSAFE COL | New York District Office (NYK-DO) |
Frequently Asked Questions
What is new honda international inc.'s FDA import refusal history?
new honda international inc. (FEI: 3013288920) has 6 FDA import refusal record(s) in our database, spanning from 1/24/2006 to 6/7/2011.
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. new honda international inc.'s FEI number is 3013288920.
What types of violations has new honda international inc. received?
new honda international inc. 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 new honda international inc. come from?
All FDA import refusal data for new honda international inc. 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.