Golden Moor
⚠️ Moderate Risk
FEI: 3000247622 • Casselman, Ontario • CANADA
FEI Number
3000247622
Location
Casselman, Ontario
Country
CANADAAddress
38 Indsutiral, , Casselman, Ontario, Canada
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
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.
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
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).
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.
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.
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).
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.
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.
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 5/7/2012 | 53LD08PASTE MASKS (MUD PACKS) (SKIN CARE PREPARATIONS) | 310POISONOUS | New York District Office (NYK-DO) |
| 9/21/2011 | 53BD99OTHER BATH PREPARATIONS, N.E.C. | 310POISONOUS | New York District Office (NYK-DO) |
| 8/5/2011 | 53BD99OTHER BATH PREPARATIONS, N.E.C. | New York District Office (NYK-DO) | |
| 8/5/2011 | 53BD99OTHER BATH PREPARATIONS, N.E.C. | New York District Office (NYK-DO) | |
| 8/5/2011 | 53LG08PASTE MASKS (MUD PACKS) (SKIN CARE PREPARATIONS) | New York District Office (NYK-DO) | |
| 8/5/2011 | 53BD99OTHER BATH PREPARATIONS, N.E.C. | New York District Office (NYK-DO) | |
| 8/5/2011 | 60LBJ99ANALGESIC, N.E.C. | New York District Office (NYK-DO) | |
| 8/5/2011 | 66VBJ99MISCELLANEOUS PATENT MEDICINES, ETC. | New York District Office (NYK-DO) | |
| 8/5/2011 | 60LBJ99ANALGESIC, N.E.C. | New York District Office (NYK-DO) | |
| 7/1/2011 | 53BG99OTHER BATH PREPARATIONS, N.E.C. | 310POISONOUS | New York District Office (NYK-DO) |
| 3/11/2011 | 53BD99OTHER BATH PREPARATIONS, N.E.C. | 310POISONOUS | New York District Office (NYK-DO) |
| 3/7/2011 | 53LG03FACE,BODY,AND HAND (EXCLUDING SHAVING PREPARATIONS) (SKIN CARE PREPARATIONS) | 473LABELING | New York District Office (NYK-DO) |
| 3/7/2011 | 53LC09SKIN FRESHENERS (SKIN CARE PREPARATIONS) | 471CSTIC LBLG | New York District Office (NYK-DO) |
| 12/16/2010 | 53LG08PASTE MASKS (MUD PACKS) (SKIN CARE PREPARATIONS) | New York District Office (NYK-DO) | |
| 12/16/2010 | 53LG08PASTE MASKS (MUD PACKS) (SKIN CARE PREPARATIONS) | New York District Office (NYK-DO) | |
| 12/10/2010 | 54FCH24SENNA (HERBAL & BOTANICALS, NOT TEAS) | 482NUTRIT LBL | Detroit District Office (DET-DO) |
| 5/24/2007 | 54YET99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C. | New York District Office (NYK-DO) | |
| 5/24/2007 | 66VOY99MISCELLANEOUS PATENT MEDICINES, ETC. | 75UNAPPROVED | New York District Office (NYK-DO) |
| 5/24/2007 | 66VOY99MISCELLANEOUS PATENT MEDICINES, ETC. | 75UNAPPROVED | New York District Office (NYK-DO) |
| 2/2/2004 | 54YBL99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C. | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Golden Moor's FDA import refusal history?
Golden Moor (FEI: 3000247622) has 20 FDA import refusal record(s) in our database, spanning from 2/2/2004 to 5/7/2012.
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. Golden Moor's FEI number is 3000247622.
What types of violations has Golden Moor received?
Golden Moor 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 Golden Moor come from?
All FDA import refusal data for Golden Moor 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.