Site records / Telangana / FEI 3005269310

Rxhomeo Private LimitedHyderabad, Telangana

FDA-registered drug establishment in Hyderabad, Telangana: label, manufacture, relabel. Registration valid to 31 Dec 2026. Record as observed 27 Sep 2026.

Inspections posted: 1
Last inspection: May 2023 · OAI
Warning letters to this FEI: 1
Import alerts at this address: 1
US border refusals, 2 years: 0

The site dossier

This site, graded.
Every fact sourced.

A grade from A to E on a registered ten-factor rubric, with the fact behind every factor
Every posted FDA citation, sorted into failure categories and set against Indian drug inspections
Warning-letter violations, numbered and labelled
Import-alert history rebuilt from the archive, each listing checked against this address
Border refusals by product, and the company's other sites, each graded
A hash of every source read, so the PDF can be checked against the record

On 2022–26 inspections the rubric never saw, grade E sites were classified OAI 26.5% of the time and grade A sites 4.0%.

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Inspections

1 FDA inspection of this FEI, by end date; 1 with a posted classification.

19 May 2023OAI · Official Action IndicatedDrug Quality Assurance · no citations posted

Warning letters and compliance actions

13 Jun 2019Warning Letter · CDER

Import alerts in force

Import-alert pages list a firm name and an address, never an FEI. Each listing under this firm's name is shown with the address FDA published and whether it is this site's.

22 May 2019Import alert 66-40 · Published address is this site SourcePublished address: 4-1-424-426 Bank Street , Hyderabad, Telangana INDIA

Registration

FEI: 3005269310
DUNS: 650833994
Registered as: Rxhomeo Private Limited
Registrant: Rxhomeo Inc
Address: Indradhanush', 4-1-424 to 426, Bank Street, Abids, Hyderabad, Telangana 500001, India (IND)
Operations: LABEL, MANUFACTURE, RELABEL
Registration expires: 31 Dec 2026

Sources: FDA drug establishment registrations, FDA Data Dashboard inspections and compliance actions, import-alert pages, warning letters, import refusals and the FDA reading room, as held in Counterfoil's point-in-time corpus. No matched action does not establish compliance, and FDA registration is not FDA approval. Sources and coverage.