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Jose Manuel Campesino Bilbao

FDA import alert and refusal historyLeon, SpainFEI 1000350175

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Example subjectJose Manuel Campesino Bilba added to Import Alert 16-129 (red list)

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As of October 26, 2026, Jose Manuel Campesino Bilbao has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on September 10, 2018, 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 Jose Manuel Campesino Bilbao

2 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
    Source

2014

  1. Inspection
    Inspection classified OAI (Official Action Indicated)Food Composition, Standards, Labeling and Econ
    Source

Questions about Jose Manuel Campesino Bilbao

Is Jose Manuel Campesino Bilbao on an FDA import alert?
No listing for Jose Manuel Campesino Bilbao 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 Jose Manuel Campesino Bilbao?
No FDA import refusals for Jose Manuel Campesino Bilbao appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was Jose Manuel Campesino Bilbao last inspected by FDA?
FDA's most recent inspection of Jose Manuel Campesino Bilbao with a final classification is dated September 10, 2018 and was classified VAI (Voluntary Action Indicated).
What is Jose Manuel Campesino Bilbao's FEI number?
Jose Manuel Campesino Bilbao's FDA Establishment Identifier (FEI) is 1000350175.

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Example subjectJose Manuel Campesino Bilba 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.