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Aimil Pharmaceutix

FDA import alert and refusal historySolan, IndiaFEI 3012127577

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Example subjectAimil Pharmaceuti added to Import Alert 16-129 (red list)

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As of October 25, 2026, Aimil Pharmaceutix is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on June 12, 2023, 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 Aimil Pharmaceutix

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

2023

  1. Import refusal
    Refused, 2 lines in one entry: Herbals & botanicals (not teas), n.e.c.UNAPPROVEDEntry AEK-3416965-4Show 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 Aimil Pharmaceutix

Is Aimil Pharmaceutix on an FDA import alert?
No listing for Aimil Pharmaceutix appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the India page.
Has FDA refused shipments from Aimil Pharmaceutix?
Yes. FDA refused 2 shipment lines from Aimil Pharmaceutix on June 12, 2023. The most recent, on June 12, 2023, was herbals & botanicals (not teas), n.e.c., charged as UNAPPROVED (unapproved new drug).
Why did FDA refuse Aimil Pharmaceutix's shipments?
The most frequent charge is UNAPPROVED (unapproved new drug, 2 lines).
What is Aimil Pharmaceutix's FEI number?
Aimil Pharmaceutix's FDA Establishment Identifier (FEI) is 3012127577.

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Example subjectAimil Pharmaceuti 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.