Menadiona S.A.

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

Refusal charges, in plain English

• DIRECTIONS1 refused line

  DIRECTIONS

• 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.

• STD IDENT1 refused line

  Does not conform to standard of identity

  The product appeared to be represented as a food that has an FDA standard of identity, but not to conform to that standard.

Questions about Menadiona S.A.

Is Menadiona S.A. on an FDA import alert?

No listing for Menadiona S.A. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Spain page.

Has FDA refused shipments from Menadiona S.A.?

Yes. FDA refused 1 shipment line from Menadiona S.A. on January 25, 2018. The most recent, on January 25, 2018, was menadione (vitamin), charged as DIRECTIONS (directions).

Why did FDA refuse Menadiona S.A.'s shipments?

The most frequent charges are DIRECTIONS (directions, 1 line) and LACKS FIRM (manufacturer name and address missing, 1 line).

When was Menadiona S.A. last inspected by FDA?

FDA's most recent inspection of Menadiona S.A. with a final classification is dated April 24, 2014 and was classified NAI (No Action Indicated).

What is Menadiona S.A.'s FEI number?

Menadiona S.A.'s FDA Establishment Identifier (FEI) is 1000242648.