Mene Et Moy Laboratoires
⚠️ Moderate Risk
FEI: 3004578777 • La Colle Sur Lo • FRANCE
FEI Number
3004578777
Location
La Colle Sur Lo
Country
FRANCEAddress
Bp 31, , La Colle Sur Lo, , France
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
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).
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.
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.
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.
LACKS N/C
The article is in package form and appears to not have a label containing an accurate statement of the quantity of the contents in terms of weight, measure or numerical count and no variations or exemptions have been prescribed by regs.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 9/21/2005 | 53LC06MOISTURIZING (SKIN CARE PREPARATIONS) | 475COSMETLBLG | New Orleans District Office (NOL-DO) |
| 9/21/2005 | 63VBJ99DEPIGMENTOR N.E.C. | 118NOT LISTED | New Orleans District Office (NOL-DO) |
| 9/21/2005 | 63VAJ99DEPIGMENTOR N.E.C. | 118NOT LISTED | New Orleans District Office (NOL-DO) |
| 9/21/2005 | 63VBJ99DEPIGMENTOR N.E.C. | 118NOT LISTED | New Orleans District Office (NOL-DO) |
| 9/14/2005 | 53LC01CLEANSING (COLD CREAMS, CLEANSING LOTIONS, LIQUIDS, PADS) (SKIN CARE PREPARATIONS) | 473LABELING | New Orleans District Office (NOL-DO) |
| 9/14/2005 | 53LC01CLEANSING (COLD CREAMS, CLEANSING LOTIONS, LIQUIDS, PADS) (SKIN CARE PREPARATIONS) | 473LABELING | New Orleans District Office (NOL-DO) |
| 9/14/2005 | 53LC01CLEANSING (COLD CREAMS, CLEANSING LOTIONS, LIQUIDS, PADS) (SKIN CARE PREPARATIONS) | New Orleans District Office (NOL-DO) | |
| 9/14/2005 | 53LC01CLEANSING (COLD CREAMS, CLEANSING LOTIONS, LIQUIDS, PADS) (SKIN CARE PREPARATIONS) | New Orleans District Office (NOL-DO) |
Frequently Asked Questions
What is Mene Et Moy Laboratoires's FDA import refusal history?
Mene Et Moy Laboratoires (FEI: 3004578777) has 8 FDA import refusal record(s) in our database, spanning from 9/14/2005 to 9/21/2005.
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. Mene Et Moy Laboratoires's FEI number is 3004578777.
What types of violations has Mene Et Moy Laboratoires received?
Mene Et Moy Laboratoires has been cited for 6 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 Mene Et Moy Laboratoires come from?
All FDA import refusal data for Mene Et Moy Laboratoires 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.