Form 483

Abryl Laboratories Private Limited Form 483, 2023-11-20

FDA issued a Form 483 to Abryl Laboratories Private Limited on 2023-11-20 with 5 public-safe observations.

483· Form 483 issuedHuman Drugs5 observations

Abryl Laboratories Private Limited · Dera Bassi SAS Nagar, India · Issued November 20, 2023

Overview

  • 5 public-safe observations are available for this inspection.
  • 5 structured CFR citations are represented.
  • 1 investigator is tied to this Form 483.

Inspectional observations

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

20 Nov 2023
21 CFR 211.110(a)

Control procedures to monitor and validate performance

Cited by Kellia N Hicks

20 Nov 2023
21 CFR 211.192

Investigations of discrepancies, failures

Cited by Kellia N Hicks

20 Nov 2023
21 CFR 211.194(a)(4)

Complete Test Data

Cited by Kellia N Hicks

20 Nov 2023
21 CFR 211.22(d)

Procedures not in writing, fully followed

Cited by Kellia N Hicks

20 Nov 2023
21 CFR 211.25(a)

Training--operations, GMPs, written procedures

Cited by Kellia N Hicks

Inspected site

ALAbryl Laboratories Private LimitedDera Bassi SAS Nagar, India

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.110(a)Cited across public-safe Form 483 observations1x
21 CFR 211.192Cited across public-safe Form 483 observations1x
21 CFR 211.194(a)(4)Cited across public-safe Form 483 observations1x
21 CFR 211.22(d)Cited across public-safe Form 483 observations1x
21 CFR 211.25(a)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