Laboratoires MSP Inc.
⚠️ Moderate Risk
FEI: 3009891995 • Varennes, Quebec • CANADA
FEI Number
3009891995
Location
Varennes, Quebec
Country
CANADAAddress
2401 Montee De Picardie, , Varennes, Quebec, 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
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.
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).
DIETARYLBL
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it is a dietary supplement that appears to be misbranded within the meaning of Section 403(s)(2)(B) of the FD&C Act in that the label or labeling fails to identify the product by using the term "dietary supplement", which term may be modified with the name of such an ingredient.
UNSAFE COL
The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).
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.
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 10/29/2020 | 63RBL04SODIUM FLUORIDE (DENTAL CARIES PROPHYLACTIC) | 118NOT LISTED | Division of Northern Border Imports (DNBI) |
| 10/26/2010 | 53ED01HAIR CONDITIONERS (HAIR PREPARATIONS, NON-COLORING) | 471CSTIC LBLG | New York District Office (NYK-DO) |
| 10/26/2010 | 53ED01HAIR CONDITIONERS (HAIR PREPARATIONS, NON-COLORING) | 471CSTIC LBLG | New York District Office (NYK-DO) |
| 12/6/2007 | 53BY02BUBBLE BATHS (BATH PREPARATIONS) | 471CSTIC LBLG | New York District Office (NYK-DO) |
| 12/6/2007 | 53BY02BUBBLE BATHS (BATH PREPARATIONS) | 471CSTIC LBLG | New York District Office (NYK-DO) |
| 4/18/2006 | 53ED01HAIR CONDITIONERS (HAIR PREPARATIONS, NON-COLORING) | New York District Office (NYK-DO) | |
| 3/10/2006 | 62SBY99ANTI-SEBORRHEIC N.E.C. | 75UNAPPROVED | New York District Office (NYK-DO) |
| 3/10/2006 | 62SBL99ANTI-SEBORRHEIC N.E.C. | 75UNAPPROVED | New York District Office (NYK-DO) |
| 5/10/2002 | 54GBE01BOVINE (COW, ETC.) (ANIMAL BY-PRODUCTS AND EXTRACTS) | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Laboratoires MSP Inc.'s FDA import refusal history?
Laboratoires MSP Inc. (FEI: 3009891995) has 9 FDA import refusal record(s) in our database, spanning from 5/10/2002 to 10/29/2020.
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. Laboratoires MSP Inc.'s FEI number is 3009891995.
What types of violations has Laboratoires MSP Inc. received?
Laboratoires MSP Inc. has been cited for 7 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 Laboratoires MSP Inc. come from?
All FDA import refusal data for Laboratoires MSP 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.