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Cloetta Holland B.V.

FDA import alert and refusal historyRoosendaal, NetherlandsFEI 3004402915

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Example subjectCloetta Holland B.V added to Import Alert 16-129 (red list)

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As of October 26, 2026, Cloetta Holland B.V. is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on October 30, 2025, most often for color additive unsafe under section 721 (UNSAFE COL).

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

Current status

Import alerts
Not listed
Last import refusal
Flavored candy, soft (live savers, etc.), without nuts and fruit (without chocolate) · UNSAFE COL
Last warning letter
None found
Last inspection
Classified NAI (No Action Indicated)

Every FDA record for Cloetta Holland B.V.

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

2025

  1. Import refusal
    Refused, Flavored candy, soft (live savers, etc.), without nuts and fruit (without chocolate)UNSAFE COLEntry J21-0113862-1
    Source
  2. Inspection
    Inspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
    Source

Refusal charges, in plain English

  • UNSAFE COL1 refused line

    Color additive unsafe under section 721

    The product appeared to be, or to contain, a color additive that is unsafe within the meaning of section 721(a) of the FD&C Act, the section that governs which color additives may be used and how.

Questions about Cloetta Holland B.V.

Is Cloetta Holland B.V. on an FDA import alert?
No listing for Cloetta Holland B.V. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Netherlands page.
Has FDA refused shipments from Cloetta Holland B.V.?
Yes. FDA refused 1 shipment line from Cloetta Holland B.V. on October 30, 2025. The most recent, on October 30, 2025, was flavored candy, soft (live savers, etc.), without nuts and fruit (without chocolate), charged as UNSAFE COL (color additive unsafe under section 721).
Why did FDA refuse Cloetta Holland B.V.'s shipments?
The most frequent charge is UNSAFE COL (color additive unsafe under section 721, 1 line).
When was Cloetta Holland B.V. last inspected by FDA?
FDA's most recent inspection of Cloetta Holland B.V. with a final classification is dated January 16, 2025 and was classified NAI (No Action Indicated).
What is Cloetta Holland B.V.'s FEI number?
Cloetta Holland B.V.'s FDA Establishment Identifier (FEI) is 3004402915.

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Example subjectCloetta Holland B.V 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.