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P. Mittulaul Lalah And Sons

FDA import alert and refusal historyChennai, IndiaFEI 3004970421

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Example subjectP. Mittulaul Lalah And Son added to Import Alert 16-129 (red list)

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As of October 26, 2026, P. Mittulaul Lalah And Sons (Chennai, India) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for curry powder, liquid, without salt, 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 P. Mittulaul Lalah And Sons

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 listCurry Powder, Liquid, without Salt
    Source

Questions about P. Mittulaul Lalah And Sons

Is P. Mittulaul Lalah And Sons on an FDA import alert?
Yes. As of October 26, 2026, P. Mittulaul Lalah And Sons is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for curry powder, liquid, without salt; FDA published the listing on September 16, 2009.
Has FDA refused shipments from P. Mittulaul Lalah And Sons?
No FDA import refusals for P. Mittulaul Lalah And Sons appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is P. Mittulaul Lalah And Sons's FEI number?
P. Mittulaul Lalah And Sons's FDA Establishment Identifier (FEI) is 3004970421.
Can shipments from P. Mittulaul Lalah And Sons still enter the U.S.?
Shipments of curry powder, liquid, without salt from P. Mittulaul Lalah And Sons 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 subjectP. Mittulaul Lalah And Son 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.