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Gaivotaprateada Lda.

FDA import alert and refusal historyCondeixa A Nova, PortugalFEI 3012136889

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Example subjectGaivotaprateada Lda added to Import Alert 16-129 (red list)

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As of October 26, 2026, Gaivotaprateada Lda. is not on any FDA import alert in SupplierRadar's records; FDA refused 4 of its shipment lines on April 26, 2022, most often for filthy, putrid or decomposed substance (FILTHY).

Data from FDA public records, last checked . Request a correction

Current status

Import alerts
Not listed
Last import refusal
Octopus, other aquatic species · FILTHY
Last warning letter
None found
Last inspection
Classified NAI (No Action Indicated)

Every FDA record for Gaivotaprateada Lda.

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

2024

  1. Inspection
    Inspection classified NAI (No Action Indicated)Foodborne Biological Hazards
    Source

2022

  1. Import refusal
    Refused, 4 lines in one entry: Octopus, other aquatic speciesFILTHYEntry 406-0583192-0Show 4 lines
    • Refused, Octopus, other aquatic speciesFILTHYEntry 406-0583192-0Source
    • Refused, Octopus, other aquatic speciesFILTHYEntry 406-0583192-0Source
    • Refused, Octopus, other aquatic speciesFILTHYEntry 406-0583192-0Source
    • Refused, Octopus, other aquatic speciesFILTHYEntry 406-0583192-0Source
    Source

Refusal charges, in plain English

  • FILTHY4 refused lines

    Filthy, putrid or decomposed substance

    The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.

Questions about Gaivotaprateada Lda.

Is Gaivotaprateada Lda. on an FDA import alert?
No listing for Gaivotaprateada Lda. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Portugal page.
Has FDA refused shipments from Gaivotaprateada Lda.?
Yes. FDA refused 4 shipment lines from Gaivotaprateada Lda. on April 26, 2022. The most recent, on April 26, 2022, was octopus, other aquatic species, charged as FILTHY (filthy, putrid or decomposed substance).
Why did FDA refuse Gaivotaprateada Lda.'s shipments?
The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 4 lines).
When was Gaivotaprateada Lda. last inspected by FDA?
FDA's most recent inspection of Gaivotaprateada Lda. with a final classification is dated April 16, 2024 and was classified NAI (No Action Indicated).
What is Gaivotaprateada Lda.'s FEI number?
Gaivotaprateada Lda.'s FDA Establishment Identifier (FEI) is 3012136889.

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Example subjectGaivotaprateada Lda 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.