Visser Kaashandel B.V.

5 records, newest first. Each line links to the FDA page it came from.

Refusal charges, in plain English

• ALLERGEN1 refused line

  Major food allergen not declared

  The label appeared not to declare all major food allergens present in the product, as section 403(w) of the FD&C Act requires.

• FLAVR LBLG1 refused line

  FLAVR LBLG

• LACKS FIRM1 refused line

  Manufacturer name and address missing

  The packaged product's label appeared not to show the name and place of business of the manufacturer, packer, or distributor.

• LIST INGRE1 refused line

  Ingredients not listed

  The product is made from two or more ingredients and the label appeared not to list the common or usual name of each one (or, for a juice beverage, the percentage of juice).

• NUTRIT LBL1 refused line

  Nutrition information missing from label

  The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.

• SULFITELBL1 refused line

  SULFITELBL

• UNSAFE ADD1 refused line

  Food additive unsafe under section 409

  The product appeared to contain a food additive that is unsafe within the meaning of section 409 of the FD&C Act, the section that governs which food additives may be used and under what conditions.

Questions about Visser Kaashandel B.V.

Is Visser Kaashandel B.V. on an FDA import alert?

Yes. As of October 26, 2026, Visser Kaashandel B.V. is on the red list of FDA Import Alert 99-45, “Foods that are or contain an unsafe food additive”, for edam cheese; FDA published the listing on March 28, 2022.

Has FDA refused shipments from Visser Kaashandel B.V.?

Yes. FDA refused 2 shipment lines from Visser Kaashandel B.V. between January 18, 2017 and January 25, 2017. The most recent, on January 25, 2017, was cheese, edam, charged as LIST INGRE (ingredients not listed).

Why did FDA refuse Visser Kaashandel B.V.'s shipments?

The most frequent charges are ALLERGEN (major food allergen not declared, 1 line) and FLAVR LBLG (flavr lblg, 1 line).

When was Visser Kaashandel B.V. last inspected by FDA?

FDA's most recent inspection of Visser Kaashandel B.V. with a final classification is dated October 28, 2019 and was classified NAI (No Action Indicated).

What is Visser Kaashandel B.V.'s FEI number?

Visser Kaashandel B.V.'s FDA Establishment Identifier (FEI) is 2000000653.

Can shipments from Visser Kaashandel B.V. still enter the U.S.?

Shipments of edam cheese from Visser Kaashandel B.V. can be detained without physical examination under Import Alert 99-45; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).