Cerrado Goiano Prod Alim Ltda
⚠️ Moderate Risk
FEI: 3008849036 • Goiania • BRAZIL
FEI Number
3008849036
Location
Goiania
Country
BRAZILAddress
Rua Carmita Rezende Porto Qd 04 Lt, , Goiania, , 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)).
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
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.
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.
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 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.
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.
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 |
|---|---|---|---|
| 11/4/2011 | 37JGT99SAUCES, N.E.C. | Division of Northeast Imports (DNEI) | |
| 11/4/2011 | 21CCE99MIXED FRUIT, JAM, JELLY, PRESERVES, MARMALADE, BUTTER OR CANDIED, N.E.C. | Division of Northeast Imports (DNEI) | |
| 11/4/2011 | 26AGT09VIRGIN OLIVE OIL, CRUDE | Division of Northeast Imports (DNEI) | |
| 11/4/2011 | 26CGT05PALM KERNEL OIL, REFINED, SINGLE INGREDIENT | Division of Northeast Imports (DNEI) | |
| 11/4/2011 | 24KGT01EGG PLANT, WITH SAUCE | Division of Northeast Imports (DNEI) | |
| 11/4/2011 | 03YGT99OTHER BAKERY PRODUCTS, N.E.C. | Division of Northeast Imports (DNEI) | |
| 11/4/2011 | 28BGT05BAY (LAUREL), GROUND, CRACKED (SPICE) | Division of Northeast Imports (DNEI) | |
| 11/4/2011 | 28CGT40SAFFRON, NATURAL EXTRACT OR FLAVOR (SPICE) | Division of Northeast Imports (DNEI) | |
| 11/4/2011 | 28BGT30NUTMEG, GROUND, CRACKED (SPICE) | Division of Northeast Imports (DNEI) | |
| 11/4/2011 | 28BGT14CLOVE, GROUND, CRACKED (SPICE) | Division of Northeast Imports (DNEI) | |
| 11/4/2011 | 28BGT13CINNAMON, CASSIA, GROUND, CRACKED (SPICE) | Division of Northeast Imports (DNEI) | |
| 11/4/2011 | 28FGT99MIXED SPICE AND SEASONINGS, GROUND, CRACKED, WITHOUT SALT, N.E.C. | Division of Northeast Imports (DNEI) | |
| 11/4/2011 | 28BGT33PAPRIKA, GROUND, CRACKED (SPICE) | Division of Northeast Imports (DNEI) |
Frequently Asked Questions
What is Cerrado Goiano Prod Alim Ltda's FDA import refusal history?
Cerrado Goiano Prod Alim Ltda (FEI: 3008849036) has 13 FDA import refusal record(s) in our database, spanning from 11/4/2011 to 11/4/2011.
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. Cerrado Goiano Prod Alim Ltda's FEI number is 3008849036.
What types of violations has Cerrado Goiano Prod Alim Ltda received?
Cerrado Goiano Prod Alim Ltda 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 Cerrado Goiano Prod Alim Ltda come from?
All FDA import refusal data for Cerrado Goiano Prod Alim Ltda 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.