Indo-Marine Agencies Kerala Pvt Ltd
FDA import alert and refusal historyKochi, IndiaFEI 11185
As of October 26, 2026, Indo-Marine Agencies Kerala Pvt Ltd (Kochi, India) is on the red list of FDA Import Alert 99-37 (Low-acid canned/acidified foods without scheduled process) for prawns (shrimps) in brine; prawns in brine, published by FDA on June 3, 2014, is also listed on Import Alert 16-35 (green list), 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 99-37 · red listIA 16-35 · green list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Indo-Marine Agencies Kerala Pvt Ltd
2 records, newest first. Each line links to the FDA page it came from.
2014
- Import alert listingListed on Import Alert 99-37red listPRAWNS (SHRIMPS) IN BRINE; Prawns in brineSource
2009
- Import alert listingListed on Import Alert 16-35green listRaw ShrimpSource
Questions about Indo-Marine Agencies Kerala Pvt Ltd
- Is Indo-Marine Agencies Kerala Pvt Ltd on an FDA import alert?
- Yes. As of October 26, 2026, Indo-Marine Agencies Kerala Pvt Ltd is on the red list of FDA Import Alert 99-37, “Low-acid canned/acidified foods without scheduled process”, for prawns (shrimps) in brine; prawns in brine; FDA published the listing on June 3, 2014.
- Has FDA refused shipments from Indo-Marine Agencies Kerala Pvt Ltd?
- No FDA import refusals for Indo-Marine Agencies Kerala Pvt Ltd appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Indo-Marine Agencies Kerala Pvt Ltd's FEI number?
- Indo-Marine Agencies Kerala Pvt Ltd's FDA Establishment Identifier (FEI) is 11185.
- Can shipments from Indo-Marine Agencies Kerala Pvt Ltd still enter the U.S.?
- Shipments of prawns (shrimps) in brine; prawns in brine from Indo-Marine Agencies Kerala Pvt Ltd can be detained without physical examination under Import Alert 99-37; 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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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.