Form 483

Eugia Pharma Specialities Limited Form 483, 2016-09-16

FDA issued a Form 483 to Eugia Pharma Specialities Limited on 2016-09-16 with 8 public-safe observations.

483· Form 483 issuedHuman Drugs8 observations

Eugia Pharma Specialities Limited · Sangareddy, India · Issued September 16, 2016

Overview

  • 8 public-safe observations are available for this inspection.
  • 4 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.

16 Sep 2016
21 CFR 211.100(a)

Absence of Written Procedures

Cited by Scott T Ballard

16 Sep 2016
21 CFR 211.160(b)

Scientifically sound laboratory controls

Cited by Scott T Ballard

16 Sep 2016
21 CFR 211.160(b)(4)

Instruments, apparatus, et. al. not meeting specs

Cited by Scott T Ballard

16 Sep 2016
21 CFR 314.81(b)(1)(ii)

Contamination, chemical or physical change, deterioration

Cited by Scott T Ballard

16 Sep 2016
21 CFR 211.100(a)

Absence of Written Procedures

Cited by Scott T Ballard

Inspected site

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.100(a)Cited across public-safe Form 483 observations2x
21 CFR 211.160(b)Cited across public-safe Form 483 observations2x
21 CFR 211.160(b)(4)Cited across public-safe Form 483 observations2x
21 CFR 314.81(b)(1)(ii)Cited 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