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Khyati Global Ventures Limited

FDA import alert and refusal historyMumbai, IndiaFEI 3032274461

Recorded by FDA as KHYATI GLOBAL VENTURES LIMITED

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Example subjectKhyati Global Ventures Limite added to Import Alert 16-129 (red list)

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As of October 26, 2026, Khyati Global Ventures Limited is not on any FDA import alert in SupplierRadar's records; FDA refused 4 of its shipment lines on September 1, 2026, most often for ingredients not listed (LIST INGRE).

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

Current status

Import alerts
Not listed
Last import refusal
Mustard oil, refined, single ingredient, see 28o for mustard oil as a flavoring · UNSAFE ADD
Last warning letter
None found
Last inspection
None on record

Every FDA record for Khyati Global Ventures Limited

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

2026

  1. Import refusal
    Refused, 4 lines in one entry: Mustard oil, refined, single ingredient, see 28o for mustard oil as a flavoring; Chutney and 1 moreUNSAFE ADDHEALTH CLIST INGRELACKS N/CEntry DP4-1069528-3Show 4 lines
    Source

Refusal charges, in plain English

  • 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).

  • NEEDS FCE3 refused lines

    Processor not registered for canned or acidified foods

    The manufacturer appeared not to be registered with FDA as a low-acid canned food or acidified food processor, as 21 CFR 108.25 and 108.35 require.

  • NO PROCESS3 refused lines

    No scheduled process filed

    The manufacturer appeared not to have filed a scheduled process with FDA, which 21 CFR Part 108 requires for low-acid canned and acidified foods, so the product is treated as made under insanitary conditions.

  • LABELING2 refused lines

    Fair Packaging and Labeling Act

    The package appeared not to meet the Fair Packaging and Labeling Act because of the placement, form, or contents of a required label statement.

  • HEALTH C1 refused line

    Unauthorized nutrient content or health claim

    The label or labeling appeared to carry a nutrient content claim or health claim that is not authorized.

  • LACKS N/C1 refused line

    Net quantity statement missing

    The packaged food appeared not to carry an accurate statement of the quantity of contents, such as net weight, measure, or count, on its label.

  • NUTRIT LBL1 refused line

    Nutrition information missing from label

    The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.

  • UNSAFE ADD1 refused line

    Food additive unsafe under section 409

    The product appeared to contain a food additive that is unsafe within the meaning of section 409 of the FD&C Act, the section that governs which food additives may be used and under what conditions.

Questions about Khyati Global Ventures Limited

Is Khyati Global Ventures Limited on an FDA import alert?
No listing for Khyati Global Ventures Limited appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the India page.
Has FDA refused shipments from Khyati Global Ventures Limited?
Yes. FDA refused 4 shipment lines from Khyati Global Ventures Limited on September 1, 2026. The most recent, on September 1, 2026, was mustard oil, refined, single ingredient, see 28o for mustard oil as a flavoring, charged as UNSAFE ADD (food additive unsafe under section 409).
Why did FDA refuse Khyati Global Ventures Limited's shipments?
The most frequent charges are LIST INGRE (ingredients not listed, 3 lines) and NEEDS FCE (processor not registered for canned or acidified foods, 3 lines).
What is Khyati Global Ventures Limited's FEI number?
Khyati Global Ventures Limited's FDA Establishment Identifier (FEI) is 3032274461.

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Example subjectKhyati Global Ventures Limite 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.