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Gopal Store

FDA import alert and refusal historyNew Delhi, IndiaFEI 3014480992

Recorded by FDA as GOPAL STORE

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Example subjectGopal Stor added to Import Alert 16-129 (red list)

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As of October 26, 2026, Gopal Store is not on any FDA import alert in SupplierRadar's records; FDA refused 6 of its shipment lines on June 27, 2018, 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
Roselle (herbal & botanicals, not teas ii) · UNAPPROVED
Last warning letter
None found
Last inspection
None on record

Every FDA record for Gopal Store

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

2018

  1. Import refusal
    Refused, 6 lines in one entry: Roselle (herbal & botanicals, not teas ii); Vitamin, n.e.c.UNAPPROVEDEntry 799-6611708-4Show 6 lines
    Source

Refusal charges, in plain English

  • UNAPPROVED6 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 Gopal Store

Is Gopal Store on an FDA import alert?
No listing for Gopal Store 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 Gopal Store?
Yes. FDA refused 6 shipment lines from Gopal Store on June 27, 2018. The most recent, on June 27, 2018, was roselle (herbal & botanicals, not teas ii), charged as UNAPPROVED (unapproved new drug).
Why did FDA refuse Gopal Store's shipments?
The most frequent charge is UNAPPROVED (unapproved new drug, 6 lines).
What is Gopal Store's FEI number?
Gopal Store's FDA Establishment Identifier (FEI) is 3014480992.

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Example subjectGopal Stor 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.