The National Factory
⚠️ Moderate Risk
FEI: 1000398370 • Medina Munawara • SAUDI ARABIA
FEI Number
1000398370
Location
Medina Munawara
Country
SAUDI ARABIAAddress
Po Box 1458, , Medina Munawara, , Saudi Arabia
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.
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
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)).
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.
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.
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)).
PESTICIDES
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be adulterated because it contains a pesticide chemical, which is in violation of section 402(a)(2)(B). Contains:
UNSAFE ADD
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain an unsafe food additive within the meaning of section 409.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 4/15/2005 | 21GFT05DATES (PIT FRUIT), (PIT FRUIT) | 2920PESTICIDES | Los Angeles District Office (LOS-DO) |
| 1/7/2005 | 21GFT05DATES (PIT FRUIT), (PIT FRUIT) | 2920PESTICIDES | Los Angeles District Office (LOS-DO) |
| 2/12/2004 | 21HGH05DATES, DRIED OR PASTE | Chicago District Office (CHI-DO) | |
| 2/12/2004 | 21HEH05DATES, DRIED OR PASTE | Chicago District Office (CHI-DO) | |
| 2/12/2004 | 21HGH05DATES, DRIED OR PASTE | Chicago District Office (CHI-DO) | |
| 2/12/2004 | 21HGH05DATES, DRIED OR PASTE | Chicago District Office (CHI-DO) | |
| 1/16/2004 | 21GFT06STUFFED DATES (PIT FRUIT) | Detroit District Office (DET-DO) | |
| 1/16/2004 | 21HGT05DATES, DRIED OR PASTE | Detroit District Office (DET-DO) | |
| 1/16/2004 | 21GGT06STUFFED DATES (PIT FRUIT) | Detroit District Office (DET-DO) | |
| 1/16/2004 | 21HHT05DATES, DRIED OR PASTE | Detroit District Office (DET-DO) | |
| 1/25/2002 | 21HFT05DATES, DRIED OR PASTE | New York District Office (NYK-DO) | |
| 1/25/2002 | 21HFT05DATES, DRIED OR PASTE | New York District Office (NYK-DO) | |
| 1/25/2002 | 21HFT05DATES, DRIED OR PASTE | 473LABELING | New York District Office (NYK-DO) |
| 1/25/2002 | 21HFT05DATES, DRIED OR PASTE | New York District Office (NYK-DO) |
Frequently Asked Questions
What is The National Factory's FDA import refusal history?
The National Factory (FEI: 1000398370) has 14 FDA import refusal record(s) in our database, spanning from 1/25/2002 to 4/15/2005.
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. The National Factory's FEI number is 1000398370.
What types of violations has The National Factory received?
The National Factory has been cited for 9 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 The National Factory come from?
All FDA import refusal data for The National Factory 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.