KDC/ONE Development Corporation, Inc.
⚠️ High Risk
FEI: 3003690512 • Knowlton, Quebec • CANADA
FEI Number
3003690512
Location
Knowlton, Quebec
Country
CANADAAddress
315 Knowlton Road, , Knowlton, Quebec, Canada
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable violations.
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
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).
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).
POISONOUS
The article is subject to refusal of admission pursuant Section 801(a)(3) in that The cosmetic appears to bear or contain a poisonous or deleterious substance which may render it injurious to users under the conditions prescribed in the labeling thereof, or, under such conditions of use as are customary or usual.
FRNMFGREG
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.
DIRECTIONS
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.
DRUG NAME
The article appears to be a drug and fails to bear the proprietary or established name and/or name and quantity of each active ingredient.
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
COSMETLBLG
It appears that the cosmetic consists of two or more ingredients and the label does not list the common or usual name of each ingredient.
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.
DR QUALITY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to be represented as a drug the name of which is recognized in an official compendium and its strength appears to differ from or its quality or purity appear to fall below the standards set forth in such compendium.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 11/21/2025 | 62MBQ08MENTHOL (ANTI-PRURITIC) | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 7/13/2021 | 64ABK99DISINFECTANT N.E.C. | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 9/2/2020 | 62HAL05ETHYL ALCOHOL (ANTI-MICROBIAL) | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 8/27/2020 | 66VAY99MISCELLANEOUS PATENT MEDICINES, ETC. | Division of Southeast Imports (DSEI) | |
| 11/25/2019 | 62WBY99ASTRINGENT/ANTI-PERSPIRANT N.E.C. | Division of Northern Border Imports (DNBI) | |
| 3/23/2016 | 53LD10WRINKLE SMOOTHING (SKIN CARE PREPARATIONS) | 218LIST INGRE | Cincinnati District Office (CIN-DO) |
| 9/24/2015 | 53LD10WRINKLE SMOOTHING (SKIN CARE PREPARATIONS) | 75UNAPPROVED | New York District Office (NYK-DO) |
| 9/24/2015 | 53LD10WRINKLE SMOOTHING (SKIN CARE PREPARATIONS) | 75UNAPPROVED | New York District Office (NYK-DO) |
| 9/24/2015 | 53LD10WRINKLE SMOOTHING (SKIN CARE PREPARATIONS) | 75UNAPPROVED | New York District Office (NYK-DO) |
| 9/24/2015 | 53LD10WRINKLE SMOOTHING (SKIN CARE PREPARATIONS) | 75UNAPPROVED | New York District Office (NYK-DO) |
| 9/24/2015 | 53LD10WRINKLE SMOOTHING (SKIN CARE PREPARATIONS) | 75UNAPPROVED | New York District Office (NYK-DO) |
| 9/24/2015 | 53LD10WRINKLE SMOOTHING (SKIN CARE PREPARATIONS) | 75UNAPPROVED | New York District Office (NYK-DO) |
| 9/24/2015 | 53LD10WRINKLE SMOOTHING (SKIN CARE PREPARATIONS) | 75UNAPPROVED | New York District Office (NYK-DO) |
| 4/8/2015 | 66PBJ99ULTRAVIOLET SCREEN/SUNSCREEN N.E.C. | 118NOT LISTED | New York District Office (NYK-DO) |
| 4/8/2015 | 66PBJ99ULTRAVIOLET SCREEN/SUNSCREEN N.E.C. | 118NOT LISTED | New York District Office (NYK-DO) |
| 2/10/2014 | 62WBY99ASTRINGENT/ANTI-PERSPIRANT N.E.C. | 118NOT LISTED | Detroit District Office (DET-DO) |
| 5/3/2012 | 53LY01CLEANSING (COLD CREAMS, CLEANSING LOTIONS, LIQUIDS, PADS) (SKIN CARE PREPARATIONS) | 310POISONOUS | New York District Office (NYK-DO) |
| 2/16/2012 | 62WBK99ASTRINGENT/ANTI-PERSPIRANT N.E.C. | 118NOT LISTED | New York District Office (NYK-DO) |
| 1/30/2012 | 65LBJ99PROTECTANT N.E.C. | 118NOT LISTED | New York District Office (NYK-DO) |
| 1/17/2012 | 53AD02LOTIONS, OILS, POWDERS AND CREAMS (BABY PRODUCTS) | 310POISONOUS | New York District Office (NYK-DO) |
| 6/1/2011 | 62WBY99ASTRINGENT/ANTI-PERSPIRANT N.E.C. | 118NOT LISTED | Detroit District Office (DET-DO) |
| 6/1/2011 | 62WBL99ASTRINGENT/ANTI-PERSPIRANT N.E.C. | 118NOT LISTED | Detroit District Office (DET-DO) |
| 5/26/2011 | 62WBL99ASTRINGENT/ANTI-PERSPIRANT N.E.C. | 118NOT LISTED | Detroit District Office (DET-DO) |
| 8/31/2010 | 62MBL08MENTHOL (ANTI-PRURITIC) | New York District Office (NYK-DO) | |
| 8/31/2010 | 62MBL08MENTHOL (ANTI-PRURITIC) | New York District Office (NYK-DO) | |
| 3/28/2008 | 66VBJ99MISCELLANEOUS PATENT MEDICINES, ETC. | New York District Office (NYK-DO) | |
| 11/16/2007 | 66VBJ99MISCELLANEOUS PATENT MEDICINES, ETC. | 118NOT LISTED | New York District Office (NYK-DO) |
| 11/16/2007 | 66VBJ99MISCELLANEOUS PATENT MEDICINES, ETC. | 118NOT LISTED | New York District Office (NYK-DO) |
| 9/21/2004 | 53JG02DEODORANTS (UNDERARM)(NOT ANTIPERSPIRANT) (PERSONAL CLEANLINESS) | New England District Office (NWE-DO) | |
| 10/24/2001 | 60QCS64DYCLONINE HCL (ANESTHETIC) | 115DR QUALITY | New York District Office (NYK-DO) |
Frequently Asked Questions
What is KDC/ONE Development Corporation, Inc.'s FDA import refusal history?
KDC/ONE Development Corporation, Inc. (FEI: 3003690512) has 30 FDA import refusal record(s) in our database, spanning from 10/24/2001 to 11/21/2025.
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. KDC/ONE Development Corporation, Inc.'s FEI number is 3003690512.
What types of violations has KDC/ONE Development Corporation, Inc. received?
KDC/ONE Development Corporation, Inc. has been cited for 10 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 KDC/ONE Development Corporation, Inc. come from?
All FDA import refusal data for KDC/ONE Development Corporation, Inc. 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.