FDA-Inspected Site

Dr. Reddy's Laboratories Limited

2 FDA inspections are on record for Dr. Reddy's Laboratories Limited in Pydibhimavaram, India.

483· Form 483 issued

Pydibhimavaram, India · Last updated August 15, 2026

Overview

  • 2 FDA inspections are on record.
  • 2 inspections produced a Form 483.
  • The most recent recorded inspection date is 2025-07-18.

At a glance

Inspections

2

Form 483s

2

EIRs

0

Last outcome

Form 483

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
10 Jul 2025 – 18 Jul 2025Human Drugs483View 483 →
30 Jun 2022 – 7 Jul 2022Human Drugs483View 483 →

Observations on record

Form 483 observations cited at this site, most recent first.

18 Jul 2025
21 CFR 211.110(b)

In-process materials specifications testing

Cited by Patty P Kaewussdangkul, Jigar R Patel

18 Jul 2025
21 CFR 211.113(b)

Procedures for sterile drug products

Cited by Patty P Kaewussdangkul, Jigar R Patel

18 Jul 2025
21 CFR 211.113(b)

Validation lacking for sterile drug products

Cited by Patty P Kaewussdangkul, Jigar R Patel

18 Jul 2025
21 CFR 211.165(a)

Testing and release for distribution

Cited by Patty P Kaewussdangkul, Jigar R Patel

18 Jul 2025
21 CFR 211.192

Investigations of discrepancies, failures

Cited by Patty P Kaewussdangkul, Jigar R Patel

Investigators

FDA investigators tied to this site in the record.

Recurring citations

CFR citation patterns observed across this site's inspections.

CitationWhat it coversCited
21 CFR 211.113(b)Cited across public-safe Form 483 observations5x
21 CFR 211.192Cited across public-safe Form 483 observations4x
21 CFR 211.110(b)Cited across public-safe Form 483 observations1x
21 CFR 211.165(a)Cited across public-safe Form 483 observations1x
21 CFR 211.22(d)Cited across public-safe Form 483 observations1x
21 CFR 211.63Cited across public-safe Form 483 observations1x

Full site report

Get the verbatim findings behind Dr. Reddy's Laboratories Limited's 2 Form 483s

Source PDFs and recurring CFR citations, so your team knows what this site gets cited for.

  • The site's full inspection history, with every Form 483 and its outcome
  • Warning letters and recalls tied to the company behind it
  • Whether recurring CFR citations get closed out or repeat