Hamza Jalili Company
⚠️ High Risk
FEI: 3010180773 • Mazar-e Sharif, AF-NOTA • AFGHANISTAN
FEI Number
3010180773
Location
Mazar-e Sharif, AF-NOTA
Country
AFGHANISTANAddress
Darwazi Shadyan Industrial Park, , Mazar-e Sharif, AF-NOTA, Afghanistan
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.
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:
EXCESS SUL
The article appears to contain excessive sulfites, a poisonous and deleterious substance which may render it injurious to health.
SULFITELBL
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded because 1) it appears to contain sulfites but the label fails to declare the presence of sulfites, a fact material to sulfite-sensitive individuals who must avoid the ingredient due to potential health consequences from its consumption, and 2) it appears the food is fabricated from two or more ingredients and the label does not list the common or usual name of each ingredient.
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 10/14/2016 | 21HGH01APRICOT, DRIED OR PASTE | 245EXCESS SUL | Detroit District Office (DET-DO) |
| 10/14/2016 | 21HGH01APRICOT, DRIED OR PASTE | 245EXCESS SUL | Detroit District Office (DET-DO) |
| 4/11/2016 | 21HGH01APRICOT, DRIED OR PASTE | 245EXCESS SUL | New York District Office (NYK-DO) |
| 1/25/2016 | 21HHH01APRICOT, DRIED OR PASTE | Detroit District Office (DET-DO) | |
| 1/25/2016 | 21HGH01APRICOT, DRIED OR PASTE | Detroit District Office (DET-DO) | |
| 9/24/2014 | 20BGH10RAISINS, DRIED OR PASTE | 251POISONOUS | New York District Office (NYK-DO) |
| 9/24/2014 | 20BGH10RAISINS, DRIED OR PASTE | 251POISONOUS | New York District Office (NYK-DO) |
| 9/24/2014 | 20BGH10RAISINS, DRIED OR PASTE | 251POISONOUS | New York District Office (NYK-DO) |
| 9/24/2014 | 20BGH10RAISINS, DRIED OR PASTE | 251POISONOUS | New York District Office (NYK-DO) |
| 9/24/2014 | 20BFH10RAISINS, DRIED OR PASTE | 249FILTHY | New York District Office (NYK-DO) |
| 7/16/2013 | 20BFH10RAISINS, DRIED OR PASTE | 249FILTHY | New York District Office (NYK-DO) |
| 7/16/2013 | 20BFH10RAISINS, DRIED OR PASTE | 249FILTHY | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Hamza Jalili Company's FDA import refusal history?
Hamza Jalili Company (FEI: 3010180773) has 12 FDA import refusal record(s) in our database, spanning from 7/16/2013 to 10/14/2016.
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. Hamza Jalili Company's FEI number is 3010180773.
What types of violations has Hamza Jalili Company received?
Hamza Jalili Company 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 Hamza Jalili Company come from?
All FDA import refusal data for Hamza Jalili Company 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.