Form 483

Unichem Laboratories Limited Form 483, 2024-07-15

FDA issued a Form 483 to Unichem Laboratories Limited on 2024-07-15 with 5 public-safe observations.

483· Form 483 issuedHuman Drugs5 observations

Unichem Laboratories Limited · Pilerne Bardez, India · Issued July 15, 2024

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.

15 Jul 2024
21 CFR 211.100(b)

SOPs not followed / documented

Cited by Wayne D Mcgrath, Saleem A Akhtar

15 Jul 2024
21 CFR 211.192

Investigations of discrepancies, failures

Cited by Wayne D Mcgrath, Saleem A Akhtar

15 Jul 2024
21 CFR 211.22(a)

Lack of quality control unit

Cited by Wayne D Mcgrath, Saleem A Akhtar

15 Jul 2024
21 CFR 211.22(d)

Procedures not in writing, fully followed

Cited by Wayne D Mcgrath, Saleem A Akhtar

15 Jul 2024
21 CFR 211.68(b)

Computer control of master formula records

Cited by Wayne D Mcgrath, Saleem A Akhtar

Inspected site

ULUnichem Laboratories LimitedPilerne Bardez, 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 211.192Cited across public-safe Form 483 observations1x
21 CFR 211.22(a)Cited across public-safe Form 483 observations1x
21 CFR 211.22(d)Cited across public-safe Form 483 observations1x
21 CFR 211.68(b)Cited across public-safe Form 483 observations1x

Source document

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PDF available

Form 483 source document

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Full 483 report

Get the verbatim text of all 5 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