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K.P.Overseas Manufacture & packing

FDA import alert and refusal historyNavi Mumbai, IndiaFEI 3009799351

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Example subjectK.P.Overseas Manufacture & packin added to Import Alert 16-129 (red list)

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As of October 26, 2026, K.P.Overseas Manufacture & packing (Navi Mumbai, India) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for ground coriander, published by FDA on March 22, 2013, 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
None on record

Every FDA record for K.P.Overseas Manufacture & packing

1 record, newest first. Each line links to the FDA page it came from.

2013

  1. Import alert listing
    Listed on Import Alert 99-19red listGround Coriander
    Source

Questions about K.P.Overseas Manufacture & packing

Is K.P.Overseas Manufacture & packing on an FDA import alert?
Yes. As of October 26, 2026, K.P.Overseas Manufacture & packing is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for ground coriander; FDA published the listing on March 22, 2013.
Has FDA refused shipments from K.P.Overseas Manufacture & packing?
No FDA import refusals for K.P.Overseas Manufacture & packing appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is K.P.Overseas Manufacture & packing's FEI number?
K.P.Overseas Manufacture & packing's FDA Establishment Identifier (FEI) is 3009799351.
Can shipments from K.P.Overseas Manufacture & packing still enter the U.S.?
Shipments of ground coriander from K.P.Overseas Manufacture & packing can be detained without physical examination under Import Alert 99-19; 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 subjectK.P.Overseas Manufacture & packin 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.