Greenfish Exports
⚠️ Moderate Risk
FEI: 3005370961 • Accra • GHANA
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
NUTRIT LBL
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.
LACKS FIRM
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(e)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.
LACKS N/C
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(e)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.
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.
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.
USUAL NAME
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)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 2/8/2007 | 25LGT16CASSAVA, DRIED OR PASTE | Los Angeles District Office (LOS-DO) | |
| 12/29/2006 | 09CEE16MILK, DRIED | 482NUTRIT LBL | Los Angeles District Office (LOS-DO) |
| 12/29/2006 | 25LFH12SWEET POTATO, DRIED OR PASTE | 249FILTHY | Los Angeles District Office (LOS-DO) |
| 12/29/2006 | 24FGH06SQUASH, SUMMER (FRUIT USED AS VEGETABLE) | Los Angeles District Office (LOS-DO) | |
| 12/29/2006 | 24BGB99BEAN, CORN, PEA, DRIED OR PASTE, N.E.C. (VEGETABLE) | Los Angeles District Office (LOS-DO) | |
| 12/29/2006 | 16AFH58TILAPIA | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Greenfish Exports's FDA import refusal history?
Greenfish Exports (FEI: 3005370961) has 6 FDA import refusal record(s) in our database, spanning from 12/29/2006 to 2/8/2007.
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. Greenfish Exports's FEI number is 3005370961.
What types of violations has Greenfish Exports received?
Greenfish Exports 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 Greenfish Exports come from?
All FDA import refusal data for Greenfish Exports 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.