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Anad Clinic

FDA import alert and refusal historyHaryan, IndiaFEI 3043761104

Recorded by FDA as ANAD CLINIC

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Example subjectAnad Clini added to Import Alert 16-129 (red list)

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As of October 26, 2026, Anad Clinic is not on any FDA import alert in SupplierRadar's records; FDA refused 7 of its shipment lines on May 2, 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 Anad Clinic

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

2026

  1. Import refusal
    Refused, 7 lines in one entry: Herbals & botanicals (not teas), n.e.c.; Vitamin c (ascorbic acid)UNAPPROVEDEntry 1FX-5513874-6Show 7 lines
    Source

Refusal charges, in plain English

  • 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 Anad Clinic

Is Anad Clinic on an FDA import alert?
No listing for Anad Clinic 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 Anad Clinic?
Yes. FDA refused 7 shipment lines from Anad Clinic on May 2, 2026. The most recent, on May 2, 2026, was herbals & botanicals (not teas), n.e.c., charged as UNAPPROVED (unapproved new drug).
Why did FDA refuse Anad Clinic's shipments?
The most frequent charge is UNAPPROVED (unapproved new drug, 7 lines).
What is Anad Clinic's FEI number?
Anad Clinic's FDA Establishment Identifier (FEI) is 3043761104.

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Example subjectAnad Clini 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.