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PASTIFICIO TAMMA srl

FDA import alert and refusal historyFoggia, ItalyFEI 3004284261

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Example subjectPASTIFICIO TAMMA sr added to Import Alert 16-129 (red list)

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As of October 26, 2026, PASTIFICIO TAMMA srl has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on May 24, 2023, was classified NAI (No Action Indicated).

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

Current status

Import alerts
Not listed
Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
Classified NAI (No Action Indicated)

Every FDA record for PASTIFICIO TAMMA srl

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

2023

  1. Inspection
    Inspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
    Source

2016

  1. Inspection
    Inspection classified NAI (No Action Indicated)Foodborne Biological Hazards
    Source

2012

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
    Source

Questions about PASTIFICIO TAMMA srl

Is PASTIFICIO TAMMA srl on an FDA import alert?
No listing for PASTIFICIO TAMMA 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 PASTIFICIO TAMMA srl?
No FDA import refusals for PASTIFICIO TAMMA srl appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was PASTIFICIO TAMMA srl last inspected by FDA?
FDA's most recent inspection of PASTIFICIO TAMMA srl with a final classification is dated May 24, 2023 and was classified NAI (No Action Indicated).
What is PASTIFICIO TAMMA srl's FEI number?
PASTIFICIO TAMMA srl's FDA Establishment Identifier (FEI) is 3004284261.

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Example subjectPASTIFICIO TAMMA 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.