Al-Naafay Traders
⚠️ Moderate Risk
FEI: 3003253795 • Karachi • PAKISTAN
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.
UNSAFE COL
The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).
COLOR LBLG
The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.
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.
INCONSPICU
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)).
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)).
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.
PRESRV LBL
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a chemical preservative and it fails to bear labeling stating that fact including its function.
REGISTERED
It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).
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.
NOT LISTED
It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).
NEEDS FCE
It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).
NO PROCESS
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 7/10/2003 | 20QFH99CORE FRUIT, DRIED OR PASTE, N.E.C. | Southwest Import District Office (SWI-DO) | |
| 7/10/2003 | 28BGB01ALLSPICE, GROUND, CRACKED (SPICE) | Southwest Import District Office (SWI-DO) | |
| 7/10/2003 | 28OCT99ESSENTIAL OILS FOR FLAVORING, N.E.C. | Southwest Import District Office (SWI-DO) | |
| 7/10/2003 | 27YCT05MUSTARD, PREPARED | Southwest Import District Office (SWI-DO) | |
| 7/10/2003 | 02DGT03RICE, ENRICHED PROCESSED (PACKAGED) | Southwest Import District Office (SWI-DO) | |
| 7/10/2003 | 02DGT03RICE, ENRICHED PROCESSED (PACKAGED) | Southwest Import District Office (SWI-DO) | |
| 7/10/2003 | 02AFT05RICE, CULTIVATED, WHOLE GRAIN | Southwest Import District Office (SWI-DO) | |
| 7/10/2003 | 04CGT99NOODLES AND NOODLE PRODUCTS, N.E.C. | Southwest Import District Office (SWI-DO) | |
| 7/10/2003 | 04CGT99NOODLES AND NOODLE PRODUCTS, N.E.C. | Southwest Import District Office (SWI-DO) | |
| 7/10/2003 | 28JFT02GARLIC SALT | Southwest Import District Office (SWI-DO) | |
| 7/10/2003 | 03EET03BISCUIT DOUGH | Southwest Import District Office (SWI-DO) | |
| 7/10/2003 | 03EET03BISCUIT DOUGH | Southwest Import District Office (SWI-DO) | |
| 5/14/2003 | 53CH03EYE SHADOW (EYE MAKEUP PREPARATIONS) | 471CSTIC LBLG | Southwest Import District Office (SWI-DO) |
| 5/14/2003 | 53CG03EYE SHADOW (EYE MAKEUP PREPARATIONS) | 11UNSAFE COL | Southwest Import District Office (SWI-DO) |
| 7/29/2002 | 76EFWTOOTHBRUSH, MANUAL | Chicago District Office (CHI-DO) |
Frequently Asked Questions
What is Al-Naafay Traders's FDA import refusal history?
Al-Naafay Traders (FEI: 3003253795) has 15 FDA import refusal record(s) in our database, spanning from 7/29/2002 to 7/10/2003.
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. Al-Naafay Traders's FEI number is 3003253795.
What types of violations has Al-Naafay Traders received?
Al-Naafay Traders has been cited for 14 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 Al-Naafay Traders come from?
All FDA import refusal data for Al-Naafay Traders 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.