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Improva Herbal Products

FDA import alert and refusal historyAmbethan, IndiaFEI 3013295623

Recorded by FDA as IMPROVA HERBAL PRODUCTS

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Example subjectImprova Herbal Product added to Import Alert 16-129 (red list)

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As of October 26, 2026, Improva Herbal Products (Ambethan, India) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for moringa powder, published by FDA on July 16, 2026, is also listed on Import Alert 99-39 (red list), and has 6 FDA import refusals recorded since October 2016.

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

Current status

Last import refusal
Herbals & botanicals (not teas), n.e.c. · SALMONELLA
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for Improva Herbal Products

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

2026

  1. Import alert listing
    Listed on Import Alert 99-19red listMoringa Powder
    Source
  2. Import refusal
    Refused, Herbals & botanicals (not teas), n.e.c.SALMONELLAEntry KM6-3677679-1
    Source

2024

  1. Import alert listing
    Listed on Import Alert 99-39red listImprova Karela; Bitter Gourd Juice (IMPROVA HERBAL ASSORTED JUICE); Improva Amla; Indian Gooseberry Juice (IMPROVA HERBAL ASSORTED JUICE); Improva Wheat Grass Juice (IMPROVA HERBAL ASSORTED JUICE); Improva Neem; Indian Lilac Juice (IMPROVA HERBAL ASSORTED JUICE); Improva Haldi; Tumeric Juice (IMPRO…
    Source
  2. Import refusal
    Refused, 5 lines in one entry: Herbals & botanicals (not teas), n.e.c.; Purslane (herbal & botaniicals, not teas) and 1 moreFALSELIST INGREINCONSPICUEntry KM6-3626251-1Show 5 lines
    Source

2018

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

2015

  1. Inspection
    Inspection classified OAI (Official Action Indicated)Foodborne Biological Hazards
    Source

Refusal charges, in plain English

  • INCONSPICU3 refused lines

    Required information not conspicuous

    Information required on the label appeared not to be placed prominently or conspicuously enough to be read and understood by an ordinary consumer.

  • LIST INGRE3 refused lines

    Ingredients not listed

    The product is made from two or more ingredients and the label appeared not to list the common or usual name of each one (or, for a juice beverage, the percentage of juice).

  • FALSE2 refused lines

    False or misleading labeling

    The labeling appeared to be false or misleading in some particular.

  • SALMONELLA1 refused line

    Salmonella

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

Questions about Improva Herbal Products

Is Improva Herbal Products on an FDA import alert?
Yes. As of October 26, 2026, Improva Herbal Products is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for moringa powder; FDA published the listing on July 16, 2026.
Has FDA refused shipments from Improva Herbal Products?
Yes. FDA refused 6 shipment lines from Improva Herbal Products between October 7, 2024 and July 7, 2026. The most recent, on July 7, 2026, was herbals & botanicals (not teas), n.e.c., charged as SALMONELLA (salmonella).
Why did FDA refuse Improva Herbal Products's shipments?
The most frequent charges are INCONSPICU (required information not conspicuous, 3 lines) and LIST INGRE (ingredients not listed, 3 lines).
When was Improva Herbal Products last inspected by FDA?
FDA's most recent inspection of Improva Herbal Products with a final classification is dated June 19, 2018 and was classified VAI (Voluntary Action Indicated).
What is Improva Herbal Products's FEI number?
Improva Herbal Products's FDA Establishment Identifier (FEI) is 3013295623.
Can shipments from Improva Herbal Products still enter the U.S.?
Shipments of moringa powder from Improva Herbal Products 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 subjectImprova Herbal Product 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.