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Gadre Marine Export

FDA import alert and refusal historyRatnagiri, IndiaFEI 3004687984

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Example subjectGadre Marine Expor added to Import Alert 16-129 (red list)

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As of October 25, 2026, Gadre Marine Export 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 no FDA import refusals recorded since October 2016.

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

Current status

Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
Classified NAI (No Action Indicated)

Every FDA record for Gadre Marine Export

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

2018

  1. Inspection
    Inspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
    Source

2015

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

2014

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

Questions about Gadre Marine Export

Is Gadre Marine Export on an FDA import alert?
Yes. As of October 25, 2026, Gadre Marine Export is on the green list of FDA Import Alert 16-35, “Raw and cooked shrimp from India”, for raw shrimp; FDA published the listing on November 19, 2015.
Has FDA refused shipments from Gadre Marine Export?
No FDA import refusals for Gadre Marine Export appear in FDA's refusal data since October 2016, as of October 25, 2026.
When was Gadre Marine Export last inspected by FDA?
FDA's most recent inspection of Gadre Marine Export with a final classification is dated April 16, 2018 and was classified NAI (No Action Indicated).
What is Gadre Marine Export's FEI number?
Gadre Marine Export's FDA Establishment Identifier (FEI) is 3004687984.

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Example subjectGadre Marine Expor 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.