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Tartuflanghe SRL

FDA import alert and refusal historyPiobesi D'Alba, ItalyFEI 3003015180

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Example subjectTartuflanghe SR added to Import Alert 16-129 (red list)

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As of October 26, 2026, Tartuflanghe SRL has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on June 17, 2019, 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 Tartuflanghe SRL

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

2019

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

2013

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

2010

  1. Inspection
    Inspection classified OAI (Official Action Indicated)Foodborne Biological Hazards
    Source

Questions about Tartuflanghe SRL

Is Tartuflanghe SRL on an FDA import alert?
No listing for Tartuflanghe 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 Tartuflanghe SRL?
No FDA import refusals for Tartuflanghe SRL appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was Tartuflanghe SRL last inspected by FDA?
FDA's most recent inspection of Tartuflanghe SRL with a final classification is dated June 17, 2019 and was classified NAI (No Action Indicated).
What is Tartuflanghe SRL's FEI number?
Tartuflanghe SRL's FDA Establishment Identifier (FEI) is 3003015180.

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Example subjectTartuflanghe 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.