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Productos Lux, S.A.

FDA import alert and refusal historyPanama City, PanamaFEI 3004385603

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Example subjectProductos Lux, S.A added to Import Alert 16-129 (red list)

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As of October 26, 2026, Productos Lux, S.A. has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on April 1, 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 Productos Lux, S.A.

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

2019

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

2016

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

2015

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

Questions about Productos Lux, S.A.

Is Productos Lux, S.A. on an FDA import alert?
No listing for Productos Lux, S.A. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Panama page.
Has FDA refused shipments from Productos Lux, S.A.?
No FDA import refusals for Productos Lux, S.A. appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was Productos Lux, S.A. last inspected by FDA?
FDA's most recent inspection of Productos Lux, S.A. with a final classification is dated April 1, 2019 and was classified VAI (Voluntary Action Indicated).
What is Productos Lux, S.A.'s FEI number?
Productos Lux, S.A.'s FDA Establishment Identifier (FEI) is 3004385603.

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Example subjectProductos Lux, S.A 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.