ORION Corp. Iksan Plant(2)

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

Refusal charges, in plain English

• LIST INGRE2 refused lines

  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).

• 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.

Questions about ORION Corp. Iksan Plant(2)

Is ORION Corp. Iksan Plant(2) on an FDA import alert?

No listing for ORION Corp. Iksan Plant(2) appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the South Korea page.

Has FDA refused shipments from ORION Corp. Iksan Plant(2)?

Yes. FDA refused 2 shipment lines from ORION Corp. Iksan Plant(2) between January 19, 2017 and December 19, 2019. The most recent, on December 19, 2019, was jellied candy, soft (jelly beans, gum drops, etc.), without nuts and fruit (without chocolate), charged as LIST INGRE (ingredients not listed).

Why did FDA refuse ORION Corp. Iksan Plant(2)'s shipments?

The most frequent charges are LIST INGRE (ingredients not listed, 2 lines) and ALLERGEN (major food allergen not declared, 1 line).

When was ORION Corp. Iksan Plant(2) last inspected by FDA?

FDA's most recent inspection of ORION Corp. Iksan Plant(2) with a final classification is dated May 31, 2023 and was classified VAI (Voluntary Action Indicated).

What is ORION Corp. Iksan Plant(2)'s FEI number?

ORION Corp. Iksan Plant(2)'s FDA Establishment Identifier (FEI) is 3004293179.