Visser Kaashandel B.V.
⚠️ Moderate Risk
FEI: 2000000653 • Huizen, Noord-Holland • NETHERLANDS
FEI Number
2000000653
Location
Huizen, Noord-Holland
Country
NETHERLANDSAddress
Nijverheidsweg 20, , Huizen, Noord-Holland, Netherlands
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
UNSAFE ADD
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain an unsafe food additive within the meaning of section 409.
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.
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.
LACKS FIRM
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)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.
ALLERGEN
the label fails to declare all major food allergens present in the product, as required by section 403(w)(1).
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
SULFITELBL
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded because 1) it appears to contain sulfites but the label fails to declare the presence of sulfites, a fact material to sulfite-sensitive individuals who must avoid the ingredient due to potential health consequences from its consumption, and 2) it appears the food is fabricated from two or more ingredients and the label does not list the common or usual name of each ingredient.
FLAVR LBLG
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain an artificial flavoring and it fails to bear labeling stating that fact.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 1/25/2017 | 12AGO12CHEESE, EDAM | Division of West Coast Imports (DWCI) | |
| 1/18/2017 | 12AGP12CHEESE, EDAM | Division of Southeast Imports (DSEI) | |
| 4/25/2014 | 12AGP12CHEESE, EDAM | Division of Southeast Imports (DSEI) | |
| 4/11/2014 | 12AGP12CHEESE, EDAM | 238UNSAFE ADD | Division of Southeast Imports (DSEI) |
| 3/18/2014 | 12AGP12CHEESE, EDAM | 238UNSAFE ADD | Division of Southeast Imports (DSEI) |
| 12/16/2013 | 12AGP12CHEESE, EDAM | Division of Southeast Imports (DSEI) | |
| 12/12/2013 | 12AGP12CHEESE, EDAM | Division of Southeast Imports (DSEI) | |
| 11/29/2013 | 12AGP12CHEESE, EDAM | Division of Southeast Imports (DSEI) | |
| 3/21/2013 | 12AGP12CHEESE, EDAM | Division of Southeast Imports (DSEI) | |
| 2/28/2013 | 12AGP12CHEESE, EDAM | 238UNSAFE ADD | Division of Southeast Imports (DSEI) |
| 4/9/2012 | 12AGP12CHEESE, EDAM | Division of Southeast Imports (DSEI) | |
| 10/31/2011 | 12AGP12CHEESE, EDAM | 238UNSAFE ADD | Florida District Office (FLA-DO) |
Frequently Asked Questions
What is Visser Kaashandel B.V.'s FDA import refusal history?
Visser Kaashandel B.V. (FEI: 2000000653) has 12 FDA import refusal record(s) in our database, spanning from 10/31/2011 to 1/25/2017.
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. Visser Kaashandel B.V.'s FEI number is 2000000653.
What types of violations has Visser Kaashandel B.V. received?
Visser Kaashandel B.V. has been cited for 8 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 Visser Kaashandel B.V. come from?
All FDA import refusal data for Visser Kaashandel B.V. 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.