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Jairamdass Khushiram

FDA import alert and refusal historyNavi Mumbai, IndiaFEI 3012742822

Recorded by FDA as JAIRAMDASS KHUSHIRAM

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Example subjectJairamdass Khushira added to Import Alert 16-129 (red list)

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As of October 26, 2026, Jairamdass Khushiram is not on any FDA import alert in SupplierRadar's records; FDA refused 10 of its shipment lines on December 29, 2017, most often for no u.s. adverse event contact on supplement label (NCONTACT).

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

Current status

Import alerts
Not listed
Last import refusal
Tribulus (herbal & botanicals, not teas) · PLANT PART
Last warning letter
None found
Last inspection
None on record

Every FDA record for Jairamdass Khushiram

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

2017

  1. Import refusal
    Refused, 10 lines in one entry: Tribulus (herbal & botanicals, not teas); Herbals & botanicals (not teas), n.e.c. and 2 morePLANT PARTNCONTACTUNAPPROVEDEntry 799-3391544-6Show 10 lines
    Source

Refusal charges, in plain English

  • NCONTACT10 refused lines

    No U.S. adverse event contact on supplement label

    The dietary supplement label appeared not to show a U.S. address or phone number through which a serious adverse event can be reported.

  • PLANT PART8 refused lines

    PLANT PART

  • UNAPPROVED7 refused lines

    Unapproved new drug

    The product appeared to be a new drug within the meaning of section 201(p) of the FD&C Act without an approved New Drug Application. FDA can apply this charge to a food or supplement whose labeling presents it for drug uses.

Questions about Jairamdass Khushiram

Is Jairamdass Khushiram on an FDA import alert?
No listing for Jairamdass Khushiram 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 Jairamdass Khushiram?
Yes. FDA refused 10 shipment lines from Jairamdass Khushiram on December 29, 2017. The most recent, on December 29, 2017, was tribulus (herbal & botanicals, not teas), charged as PLANT PART (plant part).
Why did FDA refuse Jairamdass Khushiram's shipments?
The most frequent charges are NCONTACT (no u.s. adverse event contact on supplement label, 10 lines) and PLANT PART (plant part, 8 lines).
What is Jairamdass Khushiram's FEI number?
Jairamdass Khushiram's FDA Establishment Identifier (FEI) is 3012742822.

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Example subjectJairamdass Khushira 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.