Maimuna Corporation
⚠️ Moderate Risk
FEI: 3010242075 • Dhuliyakhal, Habiganj • BANGLADESH
FEI Number
3010242075
Location
Dhuliyakhal, Habiganj
Country
BANGLADESHAddress
Plot: B-8, 9 & 10, BSCIC Industrial Area, Dhuliyakhal, Habiganj, Bangladesh
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
PESTICIDE
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a pesticide chemical residue, which causes the article to be adulterated within the meaning of section 402(a)(2)(B) of the FD&C Act. Bears or contains:
COSMETLBLG
It appears that the cosmetic consists of two or more ingredients and the label does not list the common or usual name of each ingredient.
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
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.
CSTIC LBLG
The labeling appears to fail to comply with cosmetic labeling requirements of Section 602(a), and/or (b), and/or (c), and as identified by 21 C.F.R. Part 701.
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.
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.
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.
NO ENGLISH
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(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).
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 |
|---|---|---|---|
| 2/2/2022 | 02DGT02RICE, PLAIN (WHITE OR POLISHED) PROCESSED (PACKAGED) | 241PESTICIDE | Division of Northeast Imports (DNEI) |
| 2/2/2022 | 02DGT02RICE, PLAIN (WHITE OR POLISHED) PROCESSED (PACKAGED) | 241PESTICIDE | Division of Northeast Imports (DNEI) |
| 2/2/2022 | 02DGT02RICE, PLAIN (WHITE OR POLISHED) PROCESSED (PACKAGED) | 241PESTICIDE | Division of Northeast Imports (DNEI) |
| 2/2/2022 | 02DGT02RICE, PLAIN (WHITE OR POLISHED) PROCESSED (PACKAGED) | 241PESTICIDE | Division of Northeast Imports (DNEI) |
| 12/1/2021 | 05AGT03RICE FLAKES,PUFFS,KRISPIES,LOOPS READY TO EAT | 241PESTICIDE | Division of Northeast Imports (DNEI) |
| 6/6/2016 | 53IY02MOUTHWASHES AND BREATH FRESHENERS (LIQUIDS AND SPRAYS), WITHOUT FLUORIDE (ORAL HYGIENE PRODUCTS) | New York District Office (NYK-DO) | |
| 6/6/2016 | 53IY02MOUTHWASHES AND BREATH FRESHENERS (LIQUIDS AND SPRAYS), WITHOUT FLUORIDE (ORAL HYGIENE PRODUCTS) | New York District Office (NYK-DO) | |
| 6/6/2016 | 09AET02BUTTER OIL | New York District Office (NYK-DO) | |
| 10/5/2015 | 04CGT99NOODLES AND NOODLE PRODUCTS, N.E.C. | Division of Northeast Imports (DNEI) |
Frequently Asked Questions
What is Maimuna Corporation's FDA import refusal history?
Maimuna Corporation (FEI: 3010242075) has 9 FDA import refusal record(s) in our database, spanning from 10/5/2015 to 2/2/2022.
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. Maimuna Corporation's FEI number is 3010242075.
What types of violations has Maimuna Corporation received?
Maimuna Corporation has been cited for 11 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 Maimuna Corporation come from?
All FDA import refusal data for Maimuna Corporation 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.