Zhejiang Hailisheng Group Co., Ltd
⚠️ Moderate Risk
FEI: 3001965028 • Zhoushan City • CHINA
FEI Number
3001965028
Location
Zhoushan City
Country
CHINAAddress
No. 2 Xinjian Road, , Zhoushan City, , 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.
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
Frequently Asked Questions
What is Zhejiang Hailisheng Group Co., Ltd's FDA import refusal history?
Zhejiang Hailisheng Group Co., Ltd (FEI: 3001965028) has 2 FDA import refusal record(s) in our database, spanning from 11/29/2001 to 5/13/2002.
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. Zhejiang Hailisheng Group Co., Ltd's FEI number is 3001965028.
What types of violations has Zhejiang Hailisheng Group Co., Ltd received?
Zhejiang Hailisheng Group Co., Ltd has been cited for 2 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 Zhejiang Hailisheng Group Co., Ltd come from?
All FDA import refusal data for Zhejiang Hailisheng Group 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.