Green Co., Ltd.
⚠️ High Risk
FEI: 3009941288 • Cheongdo, Gyeongsangbuk • SOUTH KOREA
FEI Number
3009941288
Location
Cheongdo, Gyeongsangbuk
Country
SOUTH KOREAAddress
95 Haksan1-Gil, Iseo-Myeon, Cheongdo, Gyeongsangbuk, South Korea
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
MFR INJ
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the Federal Food, Drug, and Cosmetic Act (the Act) in that such article appears to have been prepared, packed, or held under insanitary conditions whereby it may have been rendered injurious to health.
MFR INSAN
The article is subject to refusal of admission pursuant to section 801(a)(1) in that the article appears to have been manufactured, processed, or packed under insanitary conditions.
POISONOUS
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a poisonous or deleterious substance which may render the article injurious to health. Contains:
POISONORD
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a poisonous or deleterious substance which would ordinarily render the article injurious to health. Contains:
LISTERIA
The article is subject to refusal of admission pursuant to Section 801(a)(3), in that the article appears to contain Listeria monocytogenes, a poisonous and deleterious substance, which may render it injurious to health.
INSANITARY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 5/12/2020 | 25PFC11ENOKITAKE MUSHROOMS, WHOLE (BUTTON) (FUNGI) | Division of Northeast Imports (DNEI) | |
| 5/12/2020 | 25PFC11ENOKITAKE MUSHROOMS, WHOLE (BUTTON) (FUNGI) | Division of Northeast Imports (DNEI) | |
| 5/12/2020 | 25PFC11ENOKITAKE MUSHROOMS, WHOLE (BUTTON) (FUNGI) | Division of Northeast Imports (DNEI) | |
| 5/12/2020 | 25PFC11ENOKITAKE MUSHROOMS, WHOLE (BUTTON) (FUNGI) | Division of Northeast Imports (DNEI) | |
| 5/12/2020 | 25PFC11ENOKITAKE MUSHROOMS, WHOLE (BUTTON) (FUNGI) | Division of Northeast Imports (DNEI) | |
| 4/30/2020 | 25PFC11ENOKITAKE MUSHROOMS, WHOLE (BUTTON) (FUNGI) | Division of West Coast Imports (DWCI) | |
| 4/30/2020 | 25PFC11ENOKITAKE MUSHROOMS, WHOLE (BUTTON) (FUNGI) | Division of West Coast Imports (DWCI) | |
| 4/30/2020 | 25PFC11ENOKITAKE MUSHROOMS, WHOLE (BUTTON) (FUNGI) | Division of West Coast Imports (DWCI) | |
| 4/30/2020 | 25PFC11ENOKITAKE MUSHROOMS, WHOLE (BUTTON) (FUNGI) | Division of West Coast Imports (DWCI) | |
| 4/30/2020 | 25PFC11ENOKITAKE MUSHROOMS, WHOLE (BUTTON) (FUNGI) | Division of West Coast Imports (DWCI) | |
| 4/15/2020 | 25PGC11ENOKITAKE MUSHROOMS, WHOLE (BUTTON) (FUNGI) | 295LISTERIA | Division of West Coast Imports (DWCI) |
| 4/15/2020 | 25PGC11ENOKITAKE MUSHROOMS, WHOLE (BUTTON) (FUNGI) | 295LISTERIA | Division of West Coast Imports (DWCI) |
| 4/15/2020 | 25PGC11ENOKITAKE MUSHROOMS, WHOLE (BUTTON) (FUNGI) | 295LISTERIA | Division of West Coast Imports (DWCI) |
Frequently Asked Questions
What is Green Co., Ltd.'s FDA import refusal history?
Green Co., Ltd. (FEI: 3009941288) has 13 FDA import refusal record(s) in our database, spanning from 4/15/2020 to 5/12/2020.
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. Green Co., Ltd.'s FEI number is 3009941288.
What types of violations has Green Co., Ltd. received?
Green Co., Ltd. has been cited for 6 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 Green Co., Ltd. come from?
All FDA import refusal data for Green 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.