Site records / Karnataka / FEI 3015283245

Biocon Biologics LimitedBengaluru, Karnataka

FDA-registered drug establishment in Bengaluru, Karnataka: analysis, api manufacture, manufacture, pack. Registration valid to 31 Dec 2026. Record as observed 27 Sep 2026.

Inspections posted
2
Last inspection
Sep 2025 · VAI
Warning letters to this FEI
0
Import alerts at this address
0
US border refusals, 2 years
1
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.

  1. 3 Sep 2025VAI · Voluntary Action IndicatedDrug Quality Assurance · no citations posted
  2. 28 Feb 2024VAI · Voluntary Action IndicatedPre-Approval Eval. of Animal Drugs and Food Additives · 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.

Form 483s released by FDA

  1. 26 Aug 2022Form 483 · 10 pages Source
  2. 3 Sep 2025Form 483 · 9 pages Source

Other registered sites of Biocon

Registration

FEI
3015283245
DUNS
675486243
Registered as
Biocon Biologics Limited
Registrant
Biocon Biologics Limited
Address
Block No. M1, M2 and M6, Q1 (QC3 and QC10) and W3, 20th KM Hosur Road, Electronics City, Bengaluru, Karnataka 560100, India (IND)
Operations
ANALYSIS, API MANUFACTURE, MANUFACTURE, PACK
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.

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