Form 483

Mylan Laboratories Limited Form 483, 2017-05-26

FDA issued a Form 483 to Mylan Laboratories Limited on 2017-05-26 with 5 public-safe observations.

483· Form 483 issuedHuman Drugs5 observations

Mylan Laboratories Limited · Aurangabad, India · Issued May 26, 2017

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.

26 May 2017
21 CFR 211.160(a)

Lab controls established, including changes

Cited by Concepcion Cruz, Eric L Dong

26 May 2017
21 CFR 211.165(e)

Test methods

Cited by Concepcion Cruz, Eric L Dong

26 May 2017
21 CFR 211.192

Investigations of discrepancies, failures

Cited by Concepcion Cruz, Eric L Dong

26 May 2017
21 CFR 211.68(b)

Computer control of master formula records

Cited by Concepcion Cruz, Eric L Dong

26 May 2017
21 CFR 314.81(b)(1)(ii)

Failure to meet specifications

Cited by Concepcion Cruz, Eric L Dong

Inspected site

MLMylan Laboratories LimitedAurangabad, India

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.160(a)Cited across public-safe Form 483 observations1x
21 CFR 211.165(e)Cited across public-safe Form 483 observations1x
21 CFR 211.192Cited across public-safe Form 483 observations1x
21 CFR 211.68(b)Cited across public-safe Form 483 observations1x
21 CFR 314.81(b)(1)(ii)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