Form 483

Dr Reddy's Laboratories Limited Form 483, 2019-01-15

FDA issued a Form 483 to Dr Reddy's Laboratories Limited on 2019-01-15 with 4 public-safe observations.

483· Form 483 issuedHuman Drugs4 observations

Dr Reddy's Laboratories Limited · Devunipalavalasa, India · Issued January 15, 2019

Overview

  • 4 public-safe observations are available for this inspection.
  • 4 structured CFR citations are represented.
  • 2 investigators are tied to this Form 483.

Inspectional observations

Each observation cites the regulation FDA found the firm out of compliance with.

15 Jan 2019
21 CFR 211.100(b)

SOPs not followed / documented

Cited by Justin A Boyd, Rumany C Penn

15 Jan 2019
21 CFR 211.160(b)

Scientifically sound laboratory controls

Cited by Justin A Boyd, Rumany C Penn

15 Jan 2019
21 CFR 211.192

Investigations of discrepancies, failures

Cited by Justin A Boyd, Rumany C Penn

15 Jan 2019
21 CFR 211.68(b)

Computer control of master formula records

Cited by Justin A Boyd, Rumany C Penn

Inspected site

DRDr Reddy's Laboratories LimitedDevunipalavalasa, India

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.100(b)Cited across public-safe Form 483 observations1x
21 CFR 211.160(b)Cited across public-safe Form 483 observations1x
21 CFR 211.192Cited across public-safe Form 483 observations1x
21 CFR 211.68(b)Cited across public-safe Form 483 observations1x

Source document

PDF
PDF available

Form 483 source document

The source document is available to authorized Atlas users.

Full 483 report

Get the verbatim text of all 4 observations

The source PDF, so your team sees exactly what was cited and how it was answered.

  • The site's full inspection history around this Form 483
  • Whether these citations escalated to a warning letter
  • The investigators involved and the citations they repeat elsewhere