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Pesquera Larosa del Mar S.A.

FDA import alert and refusal historyBarranquilla, ColombiaFEI 2000004036

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Example subjectPesquera Larosa del Mar S.A added to Import Alert 16-129 (red list)

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As of October 26, 2026, Pesquera Larosa del Mar S.A. has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on March 29, 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 Pesquera Larosa del Mar S.A.

2 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

2013

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

Questions about Pesquera Larosa del Mar S.A.

Is Pesquera Larosa del Mar S.A. on an FDA import alert?
No listing for Pesquera Larosa del Mar 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 Colombia page.
Has FDA refused shipments from Pesquera Larosa del Mar S.A.?
No FDA import refusals for Pesquera Larosa del Mar S.A. appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was Pesquera Larosa del Mar S.A. last inspected by FDA?
FDA's most recent inspection of Pesquera Larosa del Mar S.A. with a final classification is dated March 29, 2019 and was classified VAI (Voluntary Action Indicated).
What is Pesquera Larosa del Mar S.A.'s FEI number?
Pesquera Larosa del Mar S.A.'s FDA Establishment Identifier (FEI) is 2000004036.

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Example subjectPesquera Larosa del Mar 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.