FUJIAN YUEHAI AQUATIC LIMITED COMPANY
⚠️ Moderate Risk
FEI: 3013275771 • Ningde City, Fujian • CHINA
FEI Number
3013275771
Location
Ningde City, Fujian
Country
CHINAAddress
No 1 Feiluan Industry Park Jiaocheng, District, Ningde City, 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
FILTHY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.
VETDRUGRES
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a new animal drug (or conversion product thereof) that is unsafe within the meaning of Section 512. Product contains
UNSAFE ADD
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain an unsafe food additive within the meaning of section 409.
DULCIN
The article appears to bear or contain dulcin, an unsafe food additive within the meaning of Section 409
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).
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).
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.
CYCLAMATE
The article appears to bear or contain cyclamate, an unsafe food additive within the meaning of Section 409
SACCHARLBL
The article contains Saccharin, a non-nutritive sweetener, and its label or labeling fails to list it as an added ingredient
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 1/25/2017 | 16XGT99AQUACULTURE HARVESTED FISHERY/SEAFOOD PRODUCTS, N.E.C., | Division of Northeast Imports (DNEI) | |
| 4/13/2015 | 16JGH05SHRIMP & PRAWNS | Los Angeles District Office (LOS-DO) | |
| 4/1/2014 | 24VGT03BAMBOO SHOOTS, WITH SAUCE | New York District Office (NYK-DO) | |
| 4/1/2014 | 21HGH14PLUM, DRIED OR PASTE | New York District Office (NYK-DO) | |
| 8/24/2012 | 16AGD55CORVINA | 249FILTHY | Division of Northeast Imports (DNEI) |
| 8/24/2012 | 16AGD55CORVINA | 249FILTHY | Division of Northeast Imports (DNEI) |
| 8/24/2012 | 16AGD55CORVINA | 249FILTHY | Division of Northeast Imports (DNEI) |
Frequently Asked Questions
What is FUJIAN YUEHAI AQUATIC LIMITED COMPANY's FDA import refusal history?
FUJIAN YUEHAI AQUATIC LIMITED COMPANY (FEI: 3013275771) has 7 FDA import refusal record(s) in our database, spanning from 8/24/2012 to 1/25/2017.
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. FUJIAN YUEHAI AQUATIC LIMITED COMPANY's FEI number is 3013275771.
What types of violations has FUJIAN YUEHAI AQUATIC LIMITED COMPANY received?
FUJIAN YUEHAI AQUATIC LIMITED COMPANY has been cited for 9 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 FUJIAN YUEHAI AQUATIC LIMITED COMPANY come from?
All FDA import refusal data for FUJIAN YUEHAI AQUATIC LIMITED COMPANY 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.