Abraham Michael
⚠️ Moderate Risk
FEI: 3011323620 • Addis Ababa • ETHIOPIA
FEI Number
3011323620
Location
Addis Ababa
Country
ETHIOPIAAddress
W 4 K 29 H N 821, , Addis Ababa, , Ethiopia
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
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.
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.
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.
FALSE
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(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 5/7/2015 | 24AGH51PEAS | Los Angeles District Office (LOS-DO) | |
| 5/7/2015 | 28BGH99SPICES, GROUND, CRACKED, ETC., N.E.C. | Los Angeles District Office (LOS-DO) | |
| 5/7/2015 | 21TGH99SUBTROPICAL AND TROPICAL FRUIT, DRIED OR PASTE, N.E.C. | Los Angeles District Office (LOS-DO) | |
| 5/7/2015 | 24AGH51PEAS | Los Angeles District Office (LOS-DO) | |
| 5/7/2015 | 28BGH08CAPSICUMS (CAYENNE CHILI, HOT PEPPERS), GROUND, CRACKED (SPICE) | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Abraham Michael's FDA import refusal history?
Abraham Michael (FEI: 3011323620) has 5 FDA import refusal record(s) in our database, spanning from 5/7/2015 to 5/7/2015.
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. Abraham Michael's FEI number is 3011323620.
What types of violations has Abraham Michael received?
Abraham Michael has been cited for 5 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 Abraham Michael come from?
All FDA import refusal data for Abraham Michael 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.