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Ortoconserviera Cameranese

FDA import alert and refusal historyCamerano, ItalyFEI 3011286916

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Example subjectOrtoconserviera Cameranes added to Import Alert 16-129 (red list)

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As of October 26, 2026, Ortoconserviera Cameranese has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on March 7, 2017, was classified VAI (Voluntary 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 VAI (Voluntary Action Indicated)

Every FDA record for Ortoconserviera Cameranese

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

2017

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Foodborne Biological Hazards
    Source

2014

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

Questions about Ortoconserviera Cameranese

Is Ortoconserviera Cameranese on an FDA import alert?
No listing for Ortoconserviera Cameranese 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 Ortoconserviera Cameranese?
No FDA import refusals for Ortoconserviera Cameranese appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was Ortoconserviera Cameranese last inspected by FDA?
FDA's most recent inspection of Ortoconserviera Cameranese with a final classification is dated March 7, 2017 and was classified VAI (Voluntary Action Indicated).
What is Ortoconserviera Cameranese's FEI number?
Ortoconserviera Cameranese's FDA Establishment Identifier (FEI) is 3011286916.

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Example subjectOrtoconserviera Cameranes 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.