Form 483

Intas Pharmaceuticals Limited Form 483, 2015-04-07

FDA issued a Form 483 to Intas Pharmaceuticals Limited on 2015-04-07 with 8 public-safe observations.

483· Form 483 issuedHuman Drugs8 observations

Intas Pharmaceuticals Limited · Ahmedabad, India · Issued April 7, 2015

Overview

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

Inspectional observations

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

7 Apr 2015
21 CFR 211.100(b)

SOPs not followed / documented

Cited by Debra I Love, Eileen A Liu, Narong Chamkasem

7 Apr 2015
21 CFR 211.111

Establishment of time limitations

Cited by Debra I Love, Eileen A Liu, Narong Chamkasem

7 Apr 2015
21 CFR 211.113(b)

Procedures for sterile drug products

Cited by Debra I Love, Eileen A Liu, Narong Chamkasem

7 Apr 2015
21 CFR 211.192

Investigations of discrepancies, failures

Cited by Debra I Love, Eileen A Liu, Narong Chamkasem

7 Apr 2015
21 CFR 211.100(b)

SOPs not followed / documented

Cited by Debra I Love, Eileen A Liu, Narong Chamkasem

Inspected site

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 211.111Cited across public-safe Form 483 observations2x
21 CFR 211.113(b)Cited across public-safe Form 483 observations2x
21 CFR 211.192Cited across public-safe Form 483 observations2x

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 8 observations

The source PDF and 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