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Fortmatgeria Mogent, SA

FDA import alert and refusal historySant Antoni de Vilamajor, SpainFEI 3004305867

Recorded by FDA as FORTMATGERIA MOGENT, SA

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Example subjectFortmatgeria Mogent, S added to Import Alert 16-129 (red list)

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As of October 26, 2026, Fortmatgeria Mogent, SA has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on September 5, 2019, 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 Fortmatgeria Mogent, SA

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

2019

  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 Fortmatgeria Mogent, SA

Is Fortmatgeria Mogent, SA on an FDA import alert?
No listing for Fortmatgeria Mogent, SA appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Spain page.
Has FDA refused shipments from Fortmatgeria Mogent, SA?
No FDA import refusals for Fortmatgeria Mogent, SA appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was Fortmatgeria Mogent, SA last inspected by FDA?
FDA's most recent inspection of Fortmatgeria Mogent, SA with a final classification is dated September 5, 2019 and was classified VAI (Voluntary Action Indicated).
What is Fortmatgeria Mogent, SA's FEI number?
Fortmatgeria Mogent, SA's FDA Establishment Identifier (FEI) is 3004305867.

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Example subjectFortmatgeria Mogent, S 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.