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Cepromar S.A.

FDA import alert and refusal historyGuayaquil, EcuadorFEI 3004899378

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Example subjectCepromar S.A added to Import Alert 16-129 (red list)

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As of October 26, 2026, Cepromar S.A. is on the green list of FDA Import Alert 16-05, which exempts its listed products from detention without physical examination under that alert, and has 2 FDA import refusals recorded since October 2016.

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

Current status

Last import refusal
Whiting (king, northern and silver) · FILTHY
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for Cepromar S.A.

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

2023

  1. Import refusal
    Refused, Whiting (king, northern and silver)FILTHYEntry CHQ-1050306-0
    Source

2019

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

2016

  1. Import refusal
    Refused, Mahi mahiHISTAMINEFILTHYEntry E4P-0046201-0
    Source

2013

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

2012

  1. Import alert listing
    Listed on Import Alert 16-05green listMahi Mahi
    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.

  • HISTAMINE1 refused line

    Histamine

    The product appeared to contain histamine in a quantity that ordinarily makes it injurious to health.

Questions about Cepromar S.A.

Is Cepromar S.A. on an FDA import alert?
Yes. As of October 26, 2026, Cepromar S.A. is on the green list of FDA Import Alert 16-05, “Mahimahi from Ecuador and Taiwan: histamine, decomposition”, for mahi mahi; FDA published the listing on March 13, 2012.
Has FDA refused shipments from Cepromar S.A.?
Yes. FDA refused 2 shipment lines from Cepromar S.A. between December 22, 2016 and August 14, 2023. The most recent, on August 14, 2023, was whiting (king, northern and silver), charged as FILTHY (filthy, putrid or decomposed substance).
Why did FDA refuse Cepromar S.A.'s shipments?
The most frequent charges are FILTHY (filthy, putrid or decomposed substance, 2 lines) and HISTAMINE (histamine, 1 line).
When was Cepromar S.A. last inspected by FDA?
FDA's most recent inspection of Cepromar S.A. with a final classification is dated June 17, 2019 and was classified VAI (Voluntary Action Indicated).
What is Cepromar S.A.'s FEI number?
Cepromar S.A.'s FDA Establishment Identifier (FEI) is 3004899378.

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Example subjectCepromar 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.