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Everest Ayurveda

FDA import alert and refusal historyKerala, IndiaFEI 3046540003

Recorded by FDA as EVEREST AYURVEDA

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Example subjectEverest Ayurved added to Import Alert 16-129 (red list)

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As of October 26, 2026, Everest Ayurveda is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on October 8, 2026, most often for unapproved new drug (UNAPPROVED).

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

Current status

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

Every FDA record for Everest Ayurveda

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

2026

  1. Import refusal
    Refused, Ashwagandha (herbal & botanicals, not teas)UNAPPROVEDEntry AEK-9603625-4
    Source

Refusal charges, in plain English

  • UNAPPROVED1 refused line

    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 Everest Ayurveda

Is Everest Ayurveda on an FDA import alert?
No listing for Everest Ayurveda 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 Everest Ayurveda?
Yes. FDA refused 1 shipment line from Everest Ayurveda on October 8, 2026. The most recent, on October 8, 2026, was ashwagandha (herbal & botanicals, not teas), charged as UNAPPROVED (unapproved new drug).
Why did FDA refuse Everest Ayurveda's shipments?
The most frequent charge is UNAPPROVED (unapproved new drug, 1 line).
What is Everest Ayurveda's FEI number?
Everest Ayurveda's FDA Establishment Identifier (FEI) is 3046540003.

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Example subjectEverest Ayurved 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.