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le tre a srl

FDA import alert and refusal historyOspedaletto D'Alpinolo, ItalyFEI 3004682511

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As of October 26, 2026, le tre a srl is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines between March 20, 2024 and April 16, 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
Chocolate bars · FSVP VIO
Last warning letter
None found
Last inspection
None on record

Every FDA record for le tre a srl

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

2024

  1. Import refusal
    Refused, Chocolate barsFSVP VIOEntry DF4-1613869-4
    Source
  2. Import refusal
    Refused, Chocolate and cocoa products for baking, n.e.c.FSVP VIOEntry DF4-1613237-4
    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 le tre a srl

Is le tre a srl on an FDA import alert?
No listing for le tre a srl 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 le tre a srl?
Yes. FDA refused 2 shipment lines from le tre a srl between March 20, 2024 and April 16, 2024. The most recent, on April 16, 2024, was chocolate bars, charged as FSVP VIO (importer not in compliance with fsvp).
Why did FDA refuse le tre a srl's shipments?
The most frequent charge is FSVP VIO (importer not in compliance with fsvp, 2 lines).
What is le tre a srl's FEI number?
le tre a srl's FDA Establishment Identifier (FEI) is 3004682511.

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Example subjectle tre a sr 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.