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Bonizzi s.r.l.

FDA import alert and refusal historySoncino, ItalyFEI 3011979648

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Example subjectBonizzi s.r.l added to Import Alert 16-129 (red list)

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As of October 26, 2026, Bonizzi s.r.l. is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on March 12, 2018, most often for no scheduled process filed (NO PROCESS).

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

Current status

Import alerts
Not listed
Last import refusal
Cream, sweet, whipping, table, etc. · NO PROCESS
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for Bonizzi s.r.l.

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

2018

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
    Source
  2. Import refusal
    Refused, 2 lines in one entry: Cream, sweet, whipping, table, etc.NO PROCESSEntry BJM-0116198-5Show 2 lines
    Source

Refusal charges, in plain English

  • NO PROCESS2 refused lines

    No scheduled process filed

    The manufacturer appeared not to have filed a scheduled process with FDA, which 21 CFR Part 108 requires for low-acid canned and acidified foods, so the product is treated as made under insanitary conditions.

Questions about Bonizzi s.r.l.

Is Bonizzi s.r.l. on an FDA import alert?
No listing for Bonizzi s.r.l. 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 Bonizzi s.r.l.?
Yes. FDA refused 2 shipment lines from Bonizzi s.r.l. on March 12, 2018. The most recent, on March 12, 2018, was cream, sweet, whipping, table, etc., charged as NO PROCESS (no scheduled process filed).
Why did FDA refuse Bonizzi s.r.l.'s shipments?
The most frequent charge is NO PROCESS (no scheduled process filed, 2 lines).
When was Bonizzi s.r.l. last inspected by FDA?
FDA's most recent inspection of Bonizzi s.r.l. with a final classification is dated December 18, 2018 and was classified VAI (Voluntary Action Indicated).
What is Bonizzi s.r.l.'s FEI number?
Bonizzi s.r.l.'s FDA Establishment Identifier (FEI) is 3011979648.

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Example subjectBonizzi s.r.l 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.