Chereles Audieulon
⚠️ Moderate Risk
FEI: 3003155270 • Port Au Prtince • HAITI
FEI Number
3003155270
Location
Port Au Prtince
Country
HAITIAddress
Delmas 6 # 20, , Port Au Prtince, , Haiti
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 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.
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).
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).
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.
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.
DIETARY
The article purports to be or is represented for special dietary uses and its label does not appear to bear the nutritional information required by regulation.
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
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.
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).
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.
FALSE
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(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 3/10/2008 | 17AGT50SHORTENING (LARD) | Florida District Office (FLA-DO) | |
| 3/10/2008 | 38PFT19MUSHROOM BROTH, DRIED | 324NO ENGLISH | Florida District Office (FLA-DO) |
| 2/20/2008 | 63VBY02HYDROQUINONE (DEPIGMENTOR) | 75UNAPPROVED | Florida District Office (FLA-DO) |
| 8/15/2007 | 17AGT50SHORTENING (LARD) | 324NO ENGLISH | Florida District Office (FLA-DO) |
| 8/15/2007 | 26CGT05PALM KERNEL OIL, REFINED, SINGLE INGREDIENT | 260FALSE | Florida District Office (FLA-DO) |
| 8/9/2007 | 28MHY04VANILLA (VANILLIN) IMITATION FLAVOR | Florida District Office (FLA-DO) | |
| 8/9/2007 | 36BYY06MOLASSES | Florida District Office (FLA-DO) | |
| 8/9/2007 | 38JGH11CHICKEN CONSOMME AND BOUILLION, PLAIN | Florida District Office (FLA-DO) | |
| 8/9/2007 | 25RGB99MUSHROOMS AND OTHER FUNGI PRODUCTS, BROKEN OR KIBBLED, N.E.C. | Florida District Office (FLA-DO) | |
| 8/9/2007 | 26CGT05PALM KERNEL OIL, REFINED, SINGLE INGREDIENT | Florida District Office (FLA-DO) | |
| 8/9/2007 | 23KFT09QUINOA SEED (EDIBLE SEED) | Florida District Office (FLA-DO) | |
| 8/9/2007 | 56GDL99ANTIFUNGAL N.E.C. | Florida District Office (FLA-DO) | |
| 8/9/2007 | 62FBY20IODINE (ANTI-INFECTIVE, TOPICAL) | Florida District Office (FLA-DO) | |
| 8/9/2007 | 63VDY02HYDROQUINONE (DEPIGMENTOR) | Florida District Office (FLA-DO) | |
| 8/9/2007 | 63VDY02HYDROQUINONE (DEPIGMENTOR) | Florida District Office (FLA-DO) | |
| 8/9/2007 | 63VDJ02HYDROQUINONE (DEPIGMENTOR) | Florida District Office (FLA-DO) | |
| 4/17/2007 | 28CGT02ALMOND, NATURAL EXTRACT OR FLAVOR (SPICE) | 324NO ENGLISH | Florida District Office (FLA-DO) |
| 12/8/2006 | 38PFT19MUSHROOM BROTH, DRIED | 324NO ENGLISH | Florida District Office (FLA-DO) |
| 12/8/2006 | 34BFT99CHOCOLATE AND COCOA, N.E.C. | 324NO ENGLISH | Florida District Office (FLA-DO) |
| 12/8/2006 | 02HAT02CORN STARCH | 324NO ENGLISH | Florida District Office (FLA-DO) |
| 12/8/2006 | 25QFH99MUSHROOMS AND OTHER FUNGI PRODUCTS, PIECES AND STEMS, SLICED, N.E.C. | 324NO ENGLISH | Florida District Office (FLA-DO) |
| 12/8/2006 | 23KFT09QUINOA SEED (EDIBLE SEED) | 324NO ENGLISH | Florida District Office (FLA-DO) |
| 11/1/2005 | 53IC01DENTIFRICES (AEROSOL, LIQUID, TOOTHPASTES, TOOTHPOWDERS), WITHOUT FLUORIDE (ORAL HYGIENE PRODUCTS) | Florida District Office (FLA-DO) | |
| 9/15/2005 | 25QAH99MUSHROOMS AND OTHER FUNGI PRODUCTS, PIECES AND STEMS, SLICED, N.E.C. | 249FILTHY | Florida District Office (FLA-DO) |
| 9/15/2005 | 64LDJ28FLUOCINONIDE (GLUCOCORTICOID) | 118NOT LISTED | Florida District Office (FLA-DO) |
| 9/15/2005 | 62HDY99ANTI-MICROBIAL N.E.C. | 118NOT LISTED | Florida District Office (FLA-DO) |
| 8/16/2005 | 25PGH99MUSHROOMS AND OTHER FUNGI PRODUCTS, WHOLE (BUTTON), N.E.C. | 324NO ENGLISH | Florida District Office (FLA-DO) |
| 8/16/2005 | 29YCT99SOFT DRINKS AND WATERS NOT MENTIONED ELSEWHERE, N.E.C. | Florida District Office (FLA-DO) | |
| 8/16/2005 | 29YCT99SOFT DRINKS AND WATERS NOT MENTIONED ELSEWHERE, N.E.C. | Florida District Office (FLA-DO) | |
| 8/16/2005 | 29YCT99SOFT DRINKS AND WATERS NOT MENTIONED ELSEWHERE, N.E.C. | Florida District Office (FLA-DO) | |
| 7/30/2003 | 41BHT99FOODS WITH SUPPLEMENTAL NUTRIENTS ADDED, WITH OR WITHOUT ARTIFICAL SWEETNERS | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is Chereles Audieulon's FDA import refusal history?
Chereles Audieulon (FEI: 3003155270) has 31 FDA import refusal record(s) in our database, spanning from 7/30/2003 to 3/10/2008.
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. Chereles Audieulon's FEI number is 3003155270.
What types of violations has Chereles Audieulon received?
Chereles Audieulon has been cited for 13 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 Chereles Audieulon come from?
All FDA import refusal data for Chereles Audieulon 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.