Xiamen Newdali Co., Ltd.
⚠️ Moderate Risk
FEI: 3004680553 • Xia Men, Fujian • CHINA
FEI Number
3004680553
Location
Xia Men, Fujian
Country
CHINAAddress
No. 70-74 Xinhua Road, , Xia Men, Fujian, China
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
PESTICIDE
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a pesticide chemical residue, which causes the article to be adulterated within the meaning of section 402(a)(2)(B) of the FD&C Act. Bears or contains:
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.
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 |
|---|---|---|---|
| 7/27/2020 | 25PGH10FUNGUS, WHITE, WHOLE (BUTTON) (FUNGI) | 241PESTICIDE | Division of West Coast Imports (DWCI) |
| 7/27/2020 | 25PHH10FUNGUS, WHITE, WHOLE (BUTTON) (FUNGI) | 241PESTICIDE | Division of West Coast Imports (DWCI) |
| 7/27/2020 | 25PGH10FUNGUS, WHITE, WHOLE (BUTTON) (FUNGI) | 241PESTICIDE | Division of West Coast Imports (DWCI) |
| 3/9/2011 | 25QGT09FUNGUS, BLACK (CLOUD EARS), PIECES AND STEMS, SLICED | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Xiamen Newdali Co., Ltd.'s FDA import refusal history?
Xiamen Newdali Co., Ltd. (FEI: 3004680553) has 4 FDA import refusal record(s) in our database, spanning from 3/9/2011 to 7/27/2020.
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. Xiamen Newdali Co., Ltd.'s FEI number is 3004680553.
What types of violations has Xiamen Newdali Co., Ltd. received?
Xiamen Newdali 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 Xiamen Newdali Co., Ltd. come from?
All FDA import refusal data for Xiamen Newdali 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.