Mujezath Al Shifa Trading Co.
⚠️ Moderate Risk
FEI: 3011102870 • Kuwait • KUWAIT
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 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.
UNAPPROVED
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).
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.
LACKS N/C
The article is in package form and appears to not have a label containing an accurate statement of the quantity of the contents in terms of weight, measure or numerical count and no variations or exemptions have been prescribed by regs.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 3/13/2015 | 36CGE04HONEY | Division of Southeast Imports (DSEI) | |
| 3/13/2015 | 36CGE04HONEY | Division of Southeast Imports (DSEI) | |
| 3/13/2015 | 36CGE04HONEY | Division of Southeast Imports (DSEI) | |
| 3/13/2015 | 36CGE04HONEY | Division of Southeast Imports (DSEI) | |
| 3/13/2015 | 36CGE04HONEY | Division of Southeast Imports (DSEI) | |
| 3/13/2015 | 36CGE04HONEY | Division of Southeast Imports (DSEI) | |
| 3/13/2015 | 36CGE04HONEY | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is Mujezath Al Shifa Trading Co.'s FDA import refusal history?
Mujezath Al Shifa Trading Co. (FEI: 3011102870) has 7 FDA import refusal record(s) in our database, spanning from 3/13/2015 to 3/13/2015.
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. Mujezath Al Shifa Trading Co.'s FEI number is 3011102870.
What types of violations has Mujezath Al Shifa Trading Co. received?
Mujezath Al Shifa Trading Co. 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 Mujezath Al Shifa Trading Co. come from?
All FDA import refusal data for Mujezath Al Shifa Trading Co. 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.