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Shri Purshotorm Agro Industries

FDA import alert and refusal historyAhmadabad, IndiaFEI 3003567852

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Example subjectShri Purshotorm Agro Industrie added to Import Alert 16-129 (red list)

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As of October 26, 2026, Shri Purshotorm Agro Industries (Ahmadabad, India) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for cumin; ground, 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

Import alerts
IA 99-19 · red list
Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
None on record

Every FDA record for Shri Purshotorm Agro Industries

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 listCumin; Ground
    Source

Questions about Shri Purshotorm Agro Industries

Is Shri Purshotorm Agro Industries on an FDA import alert?
Yes. As of October 26, 2026, Shri Purshotorm Agro Industries is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for cumin; ground; FDA published the listing on September 16, 2009.
Has FDA refused shipments from Shri Purshotorm Agro Industries?
No FDA import refusals for Shri Purshotorm Agro Industries appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Shri Purshotorm Agro Industries's FEI number?
Shri Purshotorm Agro Industries's FDA Establishment Identifier (FEI) is 3003567852.
Can shipments from Shri Purshotorm Agro Industries still enter the U.S.?
Shipments of cumin; ground from Shri Purshotorm Agro Industries 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 subjectShri Purshotorm Agro Industrie 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.