Form 483

Aurobindo Pharma Limited Form 483, 2016-01-29

FDA issued a Form 483 to Aurobindo Pharma Limited on 2016-01-29 with 8 public-safe observations.

483· Form 483 issuedHuman Drugs8 observations

Aurobindo Pharma Limited · Jedcherla Mandal, Mahabubnagar, India · Issued January 29, 2016

Overview

  • 8 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.

29 Jan 2016
21 CFR 211.100(b)

SOPs not followed / documented

Cited by Doan T Nguyen, Toyin B Oladimeji

29 Jan 2016
21 CFR 211.192

Investigations of discrepancies, failures

Cited by Doan T Nguyen, Toyin B Oladimeji

29 Jan 2016
21 CFR 211.42(c)

Defined areas of adequate size for operations

Cited by Doan T Nguyen, Toyin B Oladimeji

29 Jan 2016
21 CFR 211.67(b)

Written procedures fail to include

Cited by Doan T Nguyen, Toyin B Oladimeji

29 Jan 2016
21 CFR 211.100(b)

SOPs not followed / documented

Cited by Doan T Nguyen, Toyin B Oladimeji

Inspected site

APAurobindo Pharma LimitedJedcherla Mandal, Mahabubnagar, 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 observations2x
21 CFR 211.192Cited across public-safe Form 483 observations2x
21 CFR 211.42(c)Cited across public-safe Form 483 observations2x
21 CFR 211.67(b)Cited across public-safe Form 483 observations2x

Source document

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Form 483 source document

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Full 483 report

Get the verbatim text of all 8 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