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Geo Aquatic Products(P) Ltd.

FDA import alert and refusal historyAlleppey, IndiaFEI 3003117637

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Example subjectGeo Aquatic Products(P) Ltd added to Import Alert 16-129 (red list)

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As of October 26, 2026, Geo Aquatic Products(P) Ltd. 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

Import alerts
IA 16-35 · green list
Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for Geo Aquatic Products(P) Ltd.

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

2013

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

2009

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

Questions about Geo Aquatic Products(P) Ltd.

Is Geo Aquatic Products(P) Ltd. on an FDA import alert?
Yes. As of October 26, 2026, Geo Aquatic Products(P) Ltd. 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 September 18, 2009.
Has FDA refused shipments from Geo Aquatic Products(P) Ltd.?
No FDA import refusals for Geo Aquatic Products(P) Ltd. appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was Geo Aquatic Products(P) Ltd. last inspected by FDA?
FDA's most recent inspection of Geo Aquatic Products(P) Ltd. with a final classification is dated September 9, 2013 and was classified VAI (Voluntary Action Indicated).
What is Geo Aquatic Products(P) Ltd.'s FEI number?
Geo Aquatic Products(P) Ltd.'s FDA Establishment Identifier (FEI) is 3003117637.

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Example subjectGeo Aquatic Products(P) Ltd 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.