Form 483

Lupin Ltd. Form 483, 2016-01-15

FDA issued a Form 483 to Lupin Ltd. on 2016-01-15 with 9 public-safe observations.

483· Form 483 issuedHuman Drugs9 observations

Lupin Ltd. · Aurangabad, India · Issued January 15, 2016

Overview

  • 9 public-safe observations are available for this inspection.
  • 3 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 2016
21 CFR 211.160(b)(1)

Samples (various types) representative, identified properly

Cited by Doan T Nguyen, Toyin B Oladimeji

15 Jan 2016
21 CFR 211.192

Investigations of discrepancies, failures

Cited by Doan T Nguyen, Toyin B Oladimeji

15 Jan 2016
21 CFR 211.84(a)

Components withheld from use pending release

Cited by Doan T Nguyen, Toyin B Oladimeji

15 Jan 2016
21 CFR 211.160(b)(1)

Samples (various types) representative, identified properly

Cited by Doan T Nguyen, Toyin B Oladimeji

15 Jan 2016
21 CFR 211.192

Investigations of discrepancies, failures

Cited by Doan T Nguyen, Toyin B Oladimeji

Inspected site

LLLupin Ltd.Aurangabad, India

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.160(b)(1)Cited across public-safe Form 483 observations3x
21 CFR 211.192Cited across public-safe Form 483 observations3x
21 CFR 211.84(a)Cited across public-safe Form 483 observations3x

Source document

PDF
PDF available

Form 483 source document

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Full 483 report

Get the verbatim text of all 9 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