Site records / Telangana / FEI 3019037664

Cohance Lifesciences LimitedRangareddy, Telangana

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

Inspections posted: 1
Last inspection: Jul 2024 · VAI
Warning letters to this FEI: 0
Import alerts at this address: 0
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.

12 Jul 2024VAI · Voluntary Action IndicatedDrug Quality Assurance, Monitoring of Marketed Animal Drugs, Feed, and Devices · 2 citations posted

Warning letters and compliance actions

30 Jan 2026Warning letter to Cohance Lifesciences Limited SourceCGMP/Finished Pharmaceuticals/Adulterated · issued to the firm name; FDA does not tie it to this FEI

Import alerts in force

No listing in force under this firm's name.

Registration

FEI: 3019037664
DUNS: 854125972
Registered as: Cohance Lifesciences Limited
Registrant: Cohance Lifesciences Limited
Address: Survey No. 99/1, Plot No-9A(1), Mamidipally Village, Balapur Mandal, Samshabad, Rangareddy, Telangana 500108, India (IND)
Operations: ANALYSIS, LABEL, MANUFACTURE, PACK, RELABEL, REPACK
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.