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Haldiram Bhujiawala (P) ltd.

FDA import alert and refusal historyKolkata, IndiaFEI 3003620891

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Example subjectHaldiram Bhujiawala (P) ltd added to Import Alert 16-129 (red list)

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As of October 26, 2026, Haldiram Bhujiawala (P) ltd. (Kolkata, India) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for badam dalmoth snack, published by FDA on September 18, 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 Haldiram Bhujiawala (P) ltd.

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

2009

  1. Import alert listing
    Listed on Import Alert 45-02red listBadam Dalmoth Snack
    Source

Questions about Haldiram Bhujiawala (P) ltd.

Is Haldiram Bhujiawala (P) ltd. on an FDA import alert?
Yes. As of October 26, 2026, Haldiram Bhujiawala (P) ltd. is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for badam dalmoth snack; FDA published the listing on September 18, 2009.
Has FDA refused shipments from Haldiram Bhujiawala (P) ltd.?
No FDA import refusals for Haldiram Bhujiawala (P) ltd. appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Haldiram Bhujiawala (P) ltd.'s FEI number?
Haldiram Bhujiawala (P) ltd.'s FDA Establishment Identifier (FEI) is 3003620891.
Can shipments from Haldiram Bhujiawala (P) ltd. still enter the U.S.?
Shipments of badam dalmoth snack from Haldiram Bhujiawala (P) ltd. can be detained without physical examination under Import Alert 45-02; 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 subjectHaldiram Bhujiawala (P) ltd 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.