Site records / Andhra Pradesh / FEI 3010823443

Azico Biophore India Private LimitedAnakapalli, Andhra Pradesh

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

Inspections posted: 3
Last inspection: Sep 2025 · 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

3 FDA inspections of this FEI, by end date; 3 with a posted classification.

5 Sep 2025VAI · Voluntary Action IndicatedDrug Quality Assurance · no citations posted
31 Jan 2019NAI · No Action IndicatedDrug Quality Assurance · no citations posted
7 Dec 2015VAI · 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.

Registration

FEI: 3010823443
DUNS: 860186984
Registered as: AZICO BIOPHORE INDIA PRIVATE LIMITED
Registrant: AZICO BIOPHORE INDIA PRIVATE LIMITED
Address: Plot No: 40/A, J.N.Pharma City, Parawada Mandal,, Anakapalli, Andhra Pradesh 531021, 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.