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Kusum Chandra Damodar & Co

FDA import alert and refusal historyNavi Mumbai, IndiaFEI 3004326696

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Example subjectKusum Chandra Damodar & C added to Import Alert 16-129 (red list)

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As of October 27, 2026, Kusum Chandra Damodar & Co (Navi Mumbai, India) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for turmeric, ground, cracked (spice), published by FDA on September 16, 2009, 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 Kusum Chandra Damodar & Co

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

2009

  1. Import alert listing
    Listed on Import Alert 99-19red listTurmeric, Ground, Cracked (Spice)
    Source

Questions about Kusum Chandra Damodar & Co

Is Kusum Chandra Damodar & Co on an FDA import alert?
Yes. As of October 27, 2026, Kusum Chandra Damodar & Co is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for turmeric, ground, cracked (spice); FDA published the listing on September 16, 2009.
Has FDA refused shipments from Kusum Chandra Damodar & Co?
No FDA import refusals for Kusum Chandra Damodar & Co appear in FDA's refusal data since October 2016, as of October 27, 2026.
What is Kusum Chandra Damodar & Co's FEI number?
Kusum Chandra Damodar & Co's FDA Establishment Identifier (FEI) is 3004326696.
Can shipments from Kusum Chandra Damodar & Co still enter the U.S.?
Shipments of turmeric, ground, cracked (spice) from Kusum Chandra Damodar & Co 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 subjectKusum Chandra Damodar & C 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.