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Shriji Herbal Product

FDA import alert and refusal historyIdar, IndiaFEI 3002923929

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Example subjectShriji Herbal Produc added to Import Alert 16-129 (red list)

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As of October 26, 2026, Shriji Herbal Product is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on February 20, 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
Herbals & botanicals (not teas), n.e.c. · UNAPPROVED
Last warning letter
None found
Last inspection
None on record

Every FDA record for Shriji Herbal Product

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

2026

  1. Import refusal
    Refused, 2 lines in one entry: Herbals & botanicals (not teas), n.e.c.UNAPPROVEDEntry AEK-9441399-2Show 2 lines
    Source

Refusal charges, in plain English

  • UNAPPROVED2 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 Shriji Herbal Product

Is Shriji Herbal Product on an FDA import alert?
No listing for Shriji Herbal Product 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 Shriji Herbal Product?
Yes. FDA refused 2 shipment lines from Shriji Herbal Product on February 20, 2026. The most recent, on February 20, 2026, was herbals & botanicals (not teas), n.e.c., charged as UNAPPROVED (unapproved new drug).
Why did FDA refuse Shriji Herbal Product's shipments?
The most frequent charge is UNAPPROVED (unapproved new drug, 2 lines).
What is Shriji Herbal Product's FEI number?
Shriji Herbal Product's FDA Establishment Identifier (FEI) is 3002923929.

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Example subjectShriji Herbal Produc 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.