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Vishwanath Subraya Kamath & So

FDA import alert and refusal historyMangalore, IndiaFEI 1000203974

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Example subjectVishwanath Subraya Kamath & S added to Import Alert 16-129 (red list)

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As of October 26, 2026, Vishwanath Subraya Kamath & So (Mangalore, India) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for cashew, shelled, 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 Vishwanath Subraya Kamath & So

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

2009

  1. Import alert listing
    Listed on Import Alert 99-08red listCashew, Shelled
    Source

Questions about Vishwanath Subraya Kamath & So

Is Vishwanath Subraya Kamath & So on an FDA import alert?
Yes. As of October 26, 2026, Vishwanath Subraya Kamath & So is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for cashew, shelled; FDA published the listing on September 16, 2009.
Has FDA refused shipments from Vishwanath Subraya Kamath & So?
No FDA import refusals for Vishwanath Subraya Kamath & So appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Vishwanath Subraya Kamath & So's FEI number?
Vishwanath Subraya Kamath & So's FDA Establishment Identifier (FEI) is 1000203974.
Can shipments from Vishwanath Subraya Kamath & So still enter the U.S.?
Shipments of cashew, shelled from Vishwanath Subraya Kamath & So can be detained without physical examination under Import Alert 99-08; 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 subjectVishwanath Subraya Kamath & S 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.