Site records / Andhra Pradesh / FEI 3012390454

Aparna Pharmaceuticals Private LimitedSrikakulam, Andhra Pradesh

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

Inspections posted: 2
Last inspection: Sep 2023 · VAI
Warning letters to this FEI: 1
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.

12 Sep 2023VAI · Voluntary Action IndicatedDrug Quality Assurance · no citations posted
15 Mar 2019OAI · Official Action IndicatedDrug Quality Assurance · no citations posted

Warning letters and compliance actions

8 Aug 2019Warning Letter · CDER

Import alerts in force

No listing in force under this firm's name.

Registration

FEI: 3012390454
DUNS: 862603023
Registered as: Aparna Pharmaceuticals Private Limited
Registrant: Aparna Pharmaceuticals Private Limited
Address: Sy. No. 78, 79, 80 & 145, Chittivalasa Village, Pydibimavaram Panchayat Ranastalam Mandal, IP Pyidibhimavaram, Srikakulam, Andhra Pradesh 532409, India (IND)
Operations: 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.