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K.N.C. Agro Limited

FDA import alert and refusal historyPurba Medinipur, IndiaFEI 3011188882

Recorded by FDA as K.N.C. AGRO LIMITED

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Example subjectK.N.C. Agro Limite added to Import Alert 16-129 (red list)

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As of October 26, 2026, K.N.C. Agro Limited is on the green list of FDA Import Alert 16-35, which exempts its listed products from detention without physical examination under that alert, and has 8 FDA import refusals recorded since October 2016.

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

Current status

Last import refusal
Shrimp and prawns, aquaculture harvested fishery/seafood products · NITROFURAN
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for K.N.C. Agro Limited

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

2026

  1. Import refusal
    Refused, 6 lines in one entry: Shrimp and prawns, aquaculture harvested fishery/seafood productsNITROFURANEntry 417-0412883-8Show 6 lines
    • Refused, Shrimp and prawns, aquaculture harvested fishery/seafood productsNITROFURANEntry 417-0412883-8Source
    • Refused, Shrimp and prawns, aquaculture harvested fishery/seafood productsNITROFURANEntry 417-0412883-8Source
    • Refused, Shrimp and prawns, aquaculture harvested fishery/seafood productsNITROFURANEntry 417-0412883-8Source
    • Refused, Shrimp and prawns, aquaculture harvested fishery/seafood productsNITROFURANEntry 417-0412883-8Source
    • Refused, Shrimp and prawns, aquaculture harvested fishery/seafood productsNITROFURANEntry 417-0412883-8Source
    • Refused, Shrimp and prawns, aquaculture harvested fishery/seafood productsNITROFURANEntry 417-0412883-8Source
    Source
  2. Import refusal
    Refused, Shrimp and prawns, aquaculture harvested fishery/seafood productsNITROFURANEntry 417-0409165-5
    Source

2024

  1. Import refusal
    Refused, Shrimp and prawns, aquaculture harvested fishery/seafood productsFILTHYEntry 417-0381840-5
    Source

2023

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
    Source

2017

  1. Import alert listing
    Listed on Import Alert 16-35green listRaw Shrimp; Cooked Shrimp
    Source

2015

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

Refusal charges, in plain English

  • NITROFURAN7 refused lines

    Nitrofurans

    The product appeared to contain nitrofurans, a class of antibiotic drugs, which are treated as an unsafe food additive under section 409 of the FD&C Act.

  • FILTHY1 refused line

    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 K.N.C. Agro Limited

Is K.N.C. Agro Limited on an FDA import alert?
Yes. As of October 26, 2026, K.N.C. Agro Limited is on the green list of FDA Import Alert 16-35, “Raw and cooked shrimp from India”, for raw shrimp; cooked shrimp; FDA published the listing on August 25, 2017.
Has FDA refused shipments from K.N.C. Agro Limited?
Yes. FDA refused 8 shipment lines from K.N.C. Agro Limited between January 2, 2024 and August 17, 2026. The most recent, on August 17, 2026, was shrimp and prawns, aquaculture harvested fishery/seafood products, charged as NITROFURAN (nitrofurans).
Why did FDA refuse K.N.C. Agro Limited's shipments?
The most frequent charges are NITROFURAN (nitrofurans, 7 lines) and FILTHY (filthy, putrid or decomposed substance, 1 line).
When was K.N.C. Agro Limited last inspected by FDA?
FDA's most recent inspection of K.N.C. Agro Limited with a final classification is dated February 10, 2023 and was classified VAI (Voluntary Action Indicated).
What is K.N.C. Agro Limited's FEI number?
K.N.C. Agro Limited's FDA Establishment Identifier (FEI) is 3011188882.

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Example subjectK.N.C. Agro Limite 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.