MERRY GROUP (HK) LTD.
⚠️ High Risk
FEI: 3015368861 • Jiang Men, Guangdong • CHINA
FEI Number
3015368861
Location
Jiang Men, Guangdong
Country
CHINAAddress
Huaxing Industrial Park, No. 28 Double Water; Peng Jiang District, Jiang Men, Guangdong, China
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable violations.
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 1/15/2021 | 25PGH99MUSHROOMS AND OTHER FUNGI PRODUCTS, WHOLE (BUTTON), N.E.C. | 249FILTHY | Division of Northeast Imports (DNEI) |
| 1/15/2021 | 25PGH99MUSHROOMS AND OTHER FUNGI PRODUCTS, WHOLE (BUTTON), N.E.C. | 249FILTHY | Division of Northeast Imports (DNEI) |
| 5/20/2020 | 21HGT16CHINESE RED DATE (JUJUBES, ZIZIPHUS JUJUBA), DRIED OR PASTE | 249FILTHY | Division of Northeast Imports (DNEI) |
| 12/9/2019 | 21HGH05DATES, DRIED OR PASTE | 249FILTHY | Division of Northeast Imports (DNEI) |
Frequently Asked Questions
What is MERRY GROUP (HK) LTD.'s FDA import refusal history?
MERRY GROUP (HK) LTD. (FEI: 3015368861) has 4 FDA import refusal record(s) in our database, spanning from 12/9/2019 to 1/15/2021.
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. MERRY GROUP (HK) LTD.'s FEI number is 3015368861.
What types of violations has MERRY GROUP (HK) LTD. received?
MERRY GROUP (HK) LTD. has been cited for 1 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 MERRY GROUP (HK) LTD. come from?
All FDA import refusal data for MERRY GROUP (HK) 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.