Site records / Telangana / FEI 3013648186

Vision Drugs Private LimitedYadadri Bhuvanagiri, Telangana

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

Inspections posted: None
Last inspection: None posted
Warning letters to this FEI: 0
Import alerts at this address: 0
US border refusals, 2 years: 0

The site dossier

The full record.
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%.

FDA has posted no classified inspection for this site, so its dossier carries no grade. It holds the rest of the record: registration, import alerts, border refusals and the company's other sites.

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Inspections

FDA has posted no inspection of this FEI. That is an absence of record, not a clean one.

Warning letters and compliance actions

16 Aug 2013Warning letter to Vision RT Ltd SourceQuality System Regulation for Medical Devices/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: 3013648186
DUNS: 650917938
Registered as: VISION DRUGS PRIVATE LIMITED
Registrant: VISION DRUGS PRIVATE LIMITED
Address: Sy. No.733, Mandollagudem (village), Choutuppal (Mandal),, Yadadri Bhuvanagiri, Telangana 508 252, 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.