Homeolife Clinic
FDA import alert and refusal historyMumbai, IndiaFEI 3032583423
Recorded by FDA as HOMEOLIFE CLINIC
As of October 26, 2026, Homeolife Clinic is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on November 1, 2024, 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
- Vitamin b1 (thiamine) · UNAPPROVED
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Homeolife Clinic
2 records, newest first. Each line links to the FDA page it came from.
2024
- Import refusalSource
Refused, 2 lines in one entry: Vitamin b1 (thiamine); Vit dUNAPPROVEDEntry AEK-5875622-0Show 2 linesHide lines
- Refused, Vitamin b1 (thiamine)UNAPPROVEDEntry AEK-5875622-0Source
- Refused, Vit dUNAPPROVEDEntry AEK-5875622-0Source
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 Homeolife Clinic
- Is Homeolife Clinic on an FDA import alert?
- No listing for Homeolife 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 Homeolife Clinic?
- Yes. FDA refused 2 shipment lines from Homeolife Clinic on November 1, 2024. The most recent, on November 1, 2024, was vitamin b1 (thiamine), charged as UNAPPROVED (unapproved new drug).
- Why did FDA refuse Homeolife Clinic's shipments?
- The most frequent charge is UNAPPROVED (unapproved new drug, 2 lines).
- What is Homeolife Clinic's FEI number?
- Homeolife Clinic's FDA Establishment Identifier (FEI) is 3032583423.
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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.