Schmidhauser, SAS
⚠️ High Risk
FEI: 3003744179 • Alex, Haute Savoie • FRANCE
FEI Number
3003744179
Location
Alex, Haute Savoie
Country
FRANCEAddress
Zone Artisanale, 375 Route Du Fier, Alex, Haute Savoie, France
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
LISTERIA
The article is subject to refusal of admission pursuant to Section 801(a)(3), in that the article appears to contain Listeria monocytogenes, a poisonous and deleterious substance, which may render it injurious to health.
INSANITARY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.
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.
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)).
FSVP VIO
The article is subject to refusal of admission pursuant to section 801(a)(3) of the Federal Food, Drug, and Cosmetic Act (FD&C Act) in that it appears that the importer (as defined in section 805 of the FD&C Act) is in violation of section 805.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 9/8/2022 | 12AGP52CHEESE, SEMISOFT | 3886FSVP VIO | Division of Northeast Imports (DNEI) |
| 9/18/2014 | 12AGP52CHEESE, SEMISOFT | New York District Office (NYK-DO) | |
| 9/16/2014 | 12AGP52CHEESE, SEMISOFT | New York District Office (NYK-DO) | |
| 2/19/2014 | 12AGP56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT) | 295LISTERIA | New York District Office (NYK-DO) |
| 2/19/2014 | 12CGP12SOFT RIPENED CHEESE MADE FROM GOAT'S MILK (E.G., CHEVRE, FETA, GOAT) | 295LISTERIA | New York District Office (NYK-DO) |
| 12/12/2013 | 12AGO56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT) | 295LISTERIA | San Francisco District Office (SAN-DO) |
| 3/25/2013 | 12CGP12SOFT RIPENED CHEESE MADE FROM GOAT'S MILK (E.G., CHEVRE, FETA, GOAT) | 295LISTERIA | San Francisco District Office (SAN-DO) |
| 12/12/2012 | 12AGP56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT) | 295LISTERIA | Division of Northeast Imports (DNEI) |
| 1/31/2005 | 12AGP52CHEESE, SEMISOFT | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Schmidhauser, SAS's FDA import refusal history?
Schmidhauser, SAS (FEI: 3003744179) has 9 FDA import refusal record(s) in our database, spanning from 1/31/2005 to 9/8/2022.
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. Schmidhauser, SAS's FEI number is 3003744179.
What types of violations has Schmidhauser, SAS received?
Schmidhauser, SAS has been cited for 5 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 Schmidhauser, SAS come from?
All FDA import refusal data for Schmidhauser, SAS 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.