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Anil & Company

FDA import alert and refusal historyNavi Mumbai, IndiaFEI 3007185619

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Example subjectAnil & Compan added to Import Alert 16-129 (red list)

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As of October 26, 2026, Anil & Company (Navi Mumbai, India) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for spicy punjabi mix; spicy farali chivda, published by FDA on October 19, 2016, and has 7 FDA import refusals recorded since October 2016.

Data from FDA public records, last checked . Request a correction

Current status

Last import refusal
Snack foods not elsewhere mentioned, n.e.c. · SALMONELLA
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for Anil & Company

11 records, newest first. Each line links to the FDA page it came from.

2023

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
    Source

2019

  1. Import refusal
    Refused, Snack foods not elsewhere mentioned, n.e.c.SALMONELLAEntry 669-4508361-7
    Source
  2. Import refusal
    Refused, Snack foods not elsewhere mentioned, n.e.c.SALMONELLAEntry KM6-3522496-7
    Source

2018

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Foodborne Biological Hazards
    Source

2017

  1. Import refusal
    Refused, 3 lines in one entry: Other bakery products, n.e.c.FILTHYEntry KM6-3509225-7Show 3 lines
    • Refused, Other bakery products, n.e.c.FILTHYEntry KM6-3509225-7Source
    • Refused, Other bakery products, n.e.c.FILTHYEntry KM6-3509225-7Source
    • Refused, Other bakery products, n.e.c.FILTHYEntry KM6-3509225-7Source
    Source
  2. Import refusal
    Refused, Snack foods not elsewhere mentioned, n.e.c.SALMONELLAEntry KM6-3502192-6
    Source

2016

  1. Import refusal
    Refused, Snack foods not elsewhere mentioned, n.e.c.SALMONELLAEntry KM6-0088782-2
    Source
  2. Import alert listing
    Listed on Import Alert 99-19red listSpicy punjabi mix; spicy farali chivda
    Source

2010

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Foodborne Biological Hazards
    Source

Refusal charges, in plain English

  • SALMONELLA4 refused lines

    Salmonella

    The product appeared to contain Salmonella, which the law treats as a poisonous and deleterious substance that may make food injurious to health.

  • FILTHY3 refused lines

    Filthy, putrid or decomposed substance

    The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.

Questions about Anil & Company

Is Anil & Company on an FDA import alert?
Yes. As of October 26, 2026, Anil & Company is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for spicy punjabi mix; spicy farali chivda; FDA published the listing on October 19, 2016.
Has FDA refused shipments from Anil & Company?
Yes. FDA refused 7 shipment lines from Anil & Company between October 26, 2016 and April 23, 2019. The most recent, on April 23, 2019, was snack foods not elsewhere mentioned, n.e.c., charged as SALMONELLA (salmonella).
Why did FDA refuse Anil & Company's shipments?
The most frequent charges are SALMONELLA (salmonella, 4 lines) and FILTHY (filthy, putrid or decomposed substance, 3 lines).
When was Anil & Company last inspected by FDA?
FDA's most recent inspection of Anil & Company with a final classification is dated January 11, 2023 and was classified VAI (Voluntary Action Indicated).
What is Anil & Company's FEI number?
Anil & Company's FDA Establishment Identifier (FEI) is 3007185619.
Can shipments from Anil & Company still enter the U.S.?
Shipments of spicy punjabi mix; spicy farali chivda from Anil & Company 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 subjectAnil & Compan 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.