Site records / Telangana / FEI 3003802255

Valens Molecules Private LimitedMedchal, Telangana

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

Inspections posted: 2
Last inspection: Nov 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

2 FDA inspections of this FEI, by end date; 2 with a posted classification.

15 Nov 2024VAI · Voluntary Action IndicatedDrug Quality Assurance · 1 citation posted
29 Jul 2016VAI · Voluntary Action IndicatedDrug Quality Assurance · no citations posted

Warning letters and compliance actions

No FDA compliance action recorded against this FEI or letter to its name.

Import alerts in force

No listing in force under this firm's name.

Other registered sites of Valens Molecules Private Limited

Valens Molecules Private LimitedHyderabad, Telangana

Registration

FEI: 3003802255
DUNS: 675596129
Registered as: Valens Molecules Private Limited
Registrant: Valens Molecules Private Limited
Address: Plot No.11, Road No. 2, Industrial Estate Medchal Malkajgiri Dist., Medchal, Telangana 501401, India (IND)
Operations: API MANUFACTURE
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.