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Indo Fisheries

FDA import alert and refusal historyMangalore, IndiaFEI 2000032399

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Example subjectIndo Fisherie added to Import Alert 16-129 (red list)

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As of October 26, 2026, Indo Fisheries (Mangalore, India) is on the red list of FDA Import Alert 16-105 (Fish products: decomposition, histamine or indole) for king snapper; pristipomoides filamentosus; mahi mahi, published by FDA on April 1, 2022, is also listed on Import Alert 16-35 (green list) and Import Alert 16-119 (red list), and has 16 FDA import refusals recorded since October 2016.

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

Current status

Last import refusal
Snapper (red, gray, malabar, etc.) · FILTHY
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for Indo Fisheries

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

2026

  1. Import refusal
    Refused, Snapper (red, gray, malabar, etc.)FILTHYEntry 406-0617316-5
    Source

2025

  1. Import refusal
    Refused, Snapper (red, gray, malabar, etc.)FILTHYEntry 406-0617179-7
    Source
  2. Import refusal
    Refused, Snapper (red, gray, malabar, etc.)FILTHYEntry 406-0616184-8
    Source

2022

  1. Import alert listing
    Listed on Import Alert 16-105red listKing Snapper; Pristipomoides filamentosus; Mahi Mahi
    Source

2019

  1. Import refusal
    Refused, Spiny lobster, rock lobsterFILTHYEntry 406-0557365-4
    Source

2017

  1. Import refusal
    Refused, 3 lines in one entry: Mahi mahiFILTHYEntry 406-0534359-5Show 3 lines
    Source
  2. Import refusal
    Refused, 3 lines in one entry: Mahi mahiFILTHYTRANSFATEntry 406-0533542-7Show 3 lines
    Source
  3. Import refusal
    Refused, 3 lines in one entry: Mahi mahiFILTHYEntry 406-0531903-3Show 3 lines
    Source
  4. Import refusal
    Refused, 3 lines in one entry: Mahi mahiFILTHYEntry 406-0531382-0Show 3 lines
    Source

2015

  1. Import alert listing
    Listed on Import Alert 16-35green listRaw Shrimp
    Source
  2. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Foodborne Biological Hazards
    Source
  3. Import alert listing
    Listed on Import Alert 16-119red listFish Products
    Source

Refusal charges, in plain English

  • FILTHY16 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.

  • TRANSFAT3 refused lines

    TRANSFAT

Questions about Indo Fisheries

Is Indo Fisheries on an FDA import alert?
Yes. As of October 26, 2026, Indo Fisheries is on the red list of FDA Import Alert 16-105, “Fish products: decomposition, histamine or indole”, for king snapper; pristipomoides filamentosus; mahi mahi; FDA published the listing on April 1, 2022.
Has FDA refused shipments from Indo Fisheries?
Yes. FDA refused 16 shipment lines from Indo Fisheries between February 13, 2017 and January 28, 2026. The most recent, on January 28, 2026, was snapper (red, gray, malabar, etc.), charged as FILTHY (filthy, putrid or decomposed substance).
Why did FDA refuse Indo Fisheries's shipments?
The most frequent charges are FILTHY (filthy, putrid or decomposed substance, 16 lines) and TRANSFAT (transfat, 3 lines).
When was Indo Fisheries last inspected by FDA?
FDA's most recent inspection of Indo Fisheries with a final classification is dated July 31, 2015 and was classified VAI (Voluntary Action Indicated).
What is Indo Fisheries's FEI number?
Indo Fisheries's FDA Establishment Identifier (FEI) is 2000032399.
Can shipments from Indo Fisheries still enter the U.S.?
Shipments of king snapper; pristipomoides filamentosus; mahi mahi from Indo Fisheries can be detained without physical examination under Import Alert 16-105; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).

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Example subjectIndo Fisherie 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.