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Aqua Farm Del Lago C.A.

FDA import alert and refusal historyMaracaibo, VenezuelaFEI 3012232155

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Example subjectAqua Farm Del Lago C.A added to Import Alert 16-129 (red list)

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As of October 26, 2026, Aqua Farm Del Lago C.A. is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on June 27, 2018, 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
Mahi mahi · FILTHY
Last warning letter
None found
Last inspection
None on record

Every FDA record for Aqua Farm Del Lago C.A.

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

2018

  1. Import refusal
    Refused, 2 lines in one entry: Mahi mahiFILTHYEntry 9UA-0231654-7Show 2 lines
    Source

Refusal charges, in plain English

  • FILTHY2 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 Aqua Farm Del Lago C.A.

Is Aqua Farm Del Lago C.A. on an FDA import alert?
No listing for Aqua Farm Del Lago C.A. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Venezuela page.
Has FDA refused shipments from Aqua Farm Del Lago C.A.?
Yes. FDA refused 2 shipment lines from Aqua Farm Del Lago C.A. on June 27, 2018. The most recent, on June 27, 2018, was mahi mahi, charged as FILTHY (filthy, putrid or decomposed substance).
Why did FDA refuse Aqua Farm Del Lago C.A.'s shipments?
The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 2 lines).
What is Aqua Farm Del Lago C.A.'s FEI number?
Aqua Farm Del Lago C.A.'s FDA Establishment Identifier (FEI) is 3012232155.

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Example subjectAqua Farm Del Lago C.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.