A & O, EAGLE DISTRIBUTORS
⚠️ Moderate Risk
FEI: 3004677527 • La Ceiba, Atlantida • HONDURAS
FEI Number
3004677527
Location
La Ceiba, Atlantida
Country
HONDURASAddress
Edificio SUTRASFCO, Avenida La Republica, , La Ceiba, Atlantida, Honduras
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)).
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.
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.
UNAPPROVED
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).
NO PERMIT
The article of milk or cream is not accompanied by a valid import milk permit, as required by the Federal Import Milk Act (21 U.S.C. 141-149).
SALMONELLA
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain Salmonella, a poisonous and deleterious substance which may render it injurious to health.
BACTERIA
The article appears to contain a poisonous and deleterious substance which may render it injurious to health. Contains
MFR INSAN
The article is subject to refusal of admission pursuant to section 801(a)(1) in that the article appears to have been manufactured, processed, or packed under insanitary conditions.
NO ENGLISH
Required label or labeling appears to not be in English in violation of 21 C.F.R. 201.15(c)(1).
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 5/27/2008 | 12YGC99CHEESE AND CHEESE PRODUCTS, NOT ELSEWHERE MENTIONED, N.E.C. | Florida District Office (FLA-DO) | |
| 6/7/2007 | 31AYT02COFFEE, GROUND | 324NO ENGLISH | Division of Southeast Imports (DSEI) |
| 6/7/2007 | 04CGT99NOODLES AND NOODLE PRODUCTS, N.E.C. | 324NO ENGLISH | Division of Southeast Imports (DSEI) |
| 6/7/2007 | 03MGT01VANILLA COOKIE,BISCUIT,WAFER DOUGH | 324NO ENGLISH | Division of Southeast Imports (DSEI) |
| 6/7/2007 | 22KET99OTHER FRUITS AND FRUIT PRODUCTS, OTHER FRUIT JUICES OR CONCENTRATES, N.E.C. | 324NO ENGLISH | Division of Southeast Imports (DSEI) |
| 6/7/2007 | 07YDE99SNACK FOODS NOT ELSEWHERE MENTIONED, N.E.C. | 324NO ENGLISH | Division of Southeast Imports (DSEI) |
| 6/7/2007 | 29BGT07SOFT DRINK, SUBTROPICAL OR TROPICAL FRUIT FLAVORED, CARBONATED | 324NO ENGLISH | Division of Southeast Imports (DSEI) |
| 8/7/2006 | 12AGO56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT) | Florida District Office (FLA-DO) | |
| 7/11/2006 | 60LRF01ACETAMINOPHEN (ANALGESIC) | Florida District Office (FLA-DO) | |
| 3/28/2006 | 16AEE33SARDINES (BRISLING, SPRATS, PILCHARDS, ETC.) | Florida District Office (FLA-DO) | |
| 3/28/2006 | 16AEE33SARDINES (BRISLING, SPRATS, PILCHARDS, ETC.) | Florida District Office (FLA-DO) | |
| 3/28/2006 | 16AEE33SARDINES (BRISLING, SPRATS, PILCHARDS, ETC.) | Florida District Office (FLA-DO) | |
| 3/28/2006 | 16AEE33SARDINES (BRISLING, SPRATS, PILCHARDS, ETC.) | Florida District Office (FLA-DO) | |
| 6/2/2005 | 12YFE99CHEESE AND CHEESE PRODUCTS, NOT ELSEWHERE MENTIONED, N.E.C. | Florida District Office (FLA-DO) | |
| 7/13/2004 | 12AMO56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT) | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is A & O, EAGLE DISTRIBUTORS's FDA import refusal history?
A & O, EAGLE DISTRIBUTORS (FEI: 3004677527) has 15 FDA import refusal record(s) in our database, spanning from 7/13/2004 to 5/27/2008.
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. A & O, EAGLE DISTRIBUTORS's FEI number is 3004677527.
What types of violations has A & O, EAGLE DISTRIBUTORS received?
A & O, EAGLE DISTRIBUTORS has been cited for 12 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 A & O, EAGLE DISTRIBUTORS come from?
All FDA import refusal data for A & O, EAGLE DISTRIBUTORS 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.