Rxhomeo Private Limited
FDA import alert and refusal historyHyderabad, IndiaFEI 3005269310
As of October 26, 2026, Rxhomeo Private Limited is not on any FDA import alert in SupplierRadar's records; FDA refused 4 of its shipment lines between March 14, 2022 and January 19, 2023, most often for drug gmps (DRUG GMPS).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Vitamin, n.e.c. · DRUG GMPS
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Rxhomeo Private Limited
4 records, newest first. Each line links to the FDA page it came from.
2023
2022
- Import refusalRefused, Comfrey (herbal & botanicals, not teas)DRUG GMPSEntry SCS-0728066-5Source
- Import refusalRefused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.SUPPL GMPEntry SCS-0248843-8Source
- Import refusalRefused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.DRUG GMPSEntry SCS-0295742-4Source
Refusal charges, in plain English
Questions about Rxhomeo Private Limited
- Is Rxhomeo Private Limited on an FDA import alert?
- No listing for Rxhomeo Private Limited 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 Rxhomeo Private Limited?
- Yes. FDA refused 4 shipment lines from Rxhomeo Private Limited between March 14, 2022 and January 19, 2023. The most recent, on January 19, 2023, was vitamin, n.e.c., charged as DRUG GMPS (drug gmps).
- Why did FDA refuse Rxhomeo Private Limited's shipments?
- The most frequent charges are DRUG GMPS (drug gmps, 3 lines) and SUPPL GMP (dietary supplement cgmp not met, 1 line).
- What is Rxhomeo Private Limited's FEI number?
- Rxhomeo Private Limited's FDA Establishment Identifier (FEI) is 3005269310.
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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.