Form 483

Aurobindo Pharma Limited Form 483, 2009-04-09

FDA issued a Form 483 to Aurobindo Pharma Limited on 2009-04-09 with 5 public-safe observations.

483· Form 483 issued5 observations

Aurobindo Pharma Limited · Medchal, India · Issued April 9, 2009

Overview

  • 5 public-safe observations are available for this inspection.
  • 5 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.

9 Apr 2009
21 CFR 211.42(a)

Buildings of Suitable Size, Construction, Location

Cited by Susan M Jackson, Michele Perry Williams

9 Apr 2009
21 CFR 211.80(b)

Handling and Storage to Prevent Contamination

Cited by Susan M Jackson, Michele Perry Williams

9 Apr 2009
21 CFR 211.113(b)

Procedures for sterile drug products

Cited by Susan M Jackson, Michele Perry Williams

9 Apr 2009
21 CFR 211.165(e)

Test methods

Cited by Susan M Jackson, Michele Perry Williams

9 Apr 2009
21 CFR 211.186(b)(9)

Complete instructions, procedures, specifications et. al.

Cited by Susan M Jackson, Michele Perry Williams

Inspected site

APAurobindo Pharma LimitedMedchal, India

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.113(b)Cited across public-safe Form 483 observations1x
21 CFR 211.165(e)Cited across public-safe Form 483 observations1x
21 CFR 211.186(b)(9)Cited across public-safe Form 483 observations1x
21 CFR 211.42(a)Cited across public-safe Form 483 observations1x
21 CFR 211.80(b)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 5 observations

Every observation in full, 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