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Cradel

FDA import alert and refusal historyVerzuolo, ItalyFEI 3012481340

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As of October 26, 2026, Cradel is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on February 9, 2024, most often for importer not in compliance with fsvp (FSVP VIO).

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

Current status

Import alerts
Not listed
Last import refusal
Plain cookies,biscuits and wafers, n.e.c. · FSVP VIO
Last warning letter
None found
Last inspection
None on record

Every FDA record for Cradel

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

2024

  1. Import refusal
    Refused, 2 lines in one entry: Plain cookies,biscuits and wafers, n.e.c.FSVP VIOEntry DF4-1613683-9Show 2 lines
    • Refused, Plain cookies,biscuits and wafers, n.e.c.FSVP VIOEntry DF4-1613683-9Source
    • Refused, Plain cookies,biscuits and wafers, n.e.c.FSVP VIOEntry DF4-1613683-9Source
    Source

Refusal charges, in plain English

  • FSVP VIO2 refused lines

    Importer not in compliance with FSVP

    The importer of record appeared not to be in compliance with the Foreign Supplier Verification Program requirements of section 805 of the FD&C Act. The charge concerns the importer's program, not a test result on the food.

Questions about Cradel

Is Cradel on an FDA import alert?
No listing for Cradel appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Italy page.
Has FDA refused shipments from Cradel?
Yes. FDA refused 2 shipment lines from Cradel on February 9, 2024. The most recent, on February 9, 2024, was plain cookies,biscuits and wafers, n.e.c., charged as FSVP VIO (importer not in compliance with fsvp).
Why did FDA refuse Cradel's shipments?
The most frequent charge is FSVP VIO (importer not in compliance with fsvp, 2 lines).
What is Cradel's FEI number?
Cradel's FDA Establishment Identifier (FEI) is 3012481340.

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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.