SupplierRadar

Zuk Zak France

FDA import alert and refusal historyMundolsheim, FranceFEI 3015423480

Recorded by FDA as ZUK ZAK FRANCE

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Example subjectZuk Zak Franc added to Import Alert 16-129 (red list)

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As of October 26, 2026, Zuk Zak France is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on August 10, 2023, most often for food additive unsafe under section 409 (UNSAFE ADD).

Data from FDA public records, last checked . Request a correction

Current status

Import alerts
Not listed
Last import refusal
Sugar products, n.e.c. · UNSAFE ADD
Last warning letter
None found
Last inspection
None on record

Every FDA record for Zuk Zak France

1 record, newest first. Each line links to the FDA page it came from.

2023

  1. Import refusal
    Refused, Sugar products, n.e.c.UNSAFE ADDEntry SCS-1842154-8
    Source

Refusal charges, in plain English

  • 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 Zuk Zak France

Is Zuk Zak France on an FDA import alert?
No listing for Zuk Zak France appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the France page.
Has FDA refused shipments from Zuk Zak France?
Yes. FDA refused 1 shipment line from Zuk Zak France on August 10, 2023. The most recent, on August 10, 2023, was sugar products, n.e.c., charged as UNSAFE ADD (food additive unsafe under section 409).
Why did FDA refuse Zuk Zak France's shipments?
The most frequent charge is UNSAFE ADD (food additive unsafe under section 409, 1 line).
What is Zuk Zak France's FEI number?
Zuk Zak France's FDA Establishment Identifier (FEI) is 3015423480.

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Example subjectZuk Zak Franc added to Import Alert 16-129 (red list)

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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.