Native Organic Products
⚠️ Moderate Risk
FEI: 3006586461 • Sertaozinho, Sao Paulo • BRAZIL
FEI Number
3006586461
Location
Sertaozinho, Sao Paulo
Country
BRAZILAddress
Rodovia Carlos Tonanni Km 97, , Sertaozinho, Sao Paulo, Brazil
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
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 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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 1/6/2011 | 31AGN02COFFEE, GROUND | 324NO ENGLISH | New Orleans District Office (NOL-DO) |
| 1/6/2011 | 26ABN09VIRGIN OLIVE OIL, CRUDE | New Orleans District Office (NOL-DO) | |
| 1/6/2011 | 26ABN09VIRGIN OLIVE OIL, CRUDE | New Orleans District Office (NOL-DO) | |
| 1/6/2011 | 21VGO12PASSION FRUIT, JUICE, MILK, CREME, DRINK OR NECTAR, SUB/TROPICAL FRUIT | New Orleans District Office (NOL-DO) | |
| 1/6/2011 | 21VGO12PASSION FRUIT, JUICE, MILK, CREME, DRINK OR NECTAR, SUB/TROPICAL FRUIT | New Orleans District Office (NOL-DO) | |
| 1/6/2011 | 20KGO06ORANGE, CITRUS FRUIT JUICES OR CONCENTRATES | New Orleans District Office (NOL-DO) | |
| 1/6/2011 | 20KGO06ORANGE, CITRUS FRUIT JUICES OR CONCENTRATES | New Orleans District Office (NOL-DO) | |
| 1/6/2011 | 03HGT99PLAIN COOKIES,BISCUITS AND WAFERS, N.E.C. | New Orleans District Office (NOL-DO) |
Frequently Asked Questions
What is Native Organic Products's FDA import refusal history?
Native Organic Products (FEI: 3006586461) has 8 FDA import refusal record(s) in our database, spanning from 1/6/2011 to 1/6/2011.
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. Native Organic Products's FEI number is 3006586461.
What types of violations has Native Organic Products received?
Native Organic Products has been cited for 2 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 Native Organic Products come from?
All FDA import refusal data for Native Organic Products 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.