Form 483

Topix Pharmaceuticals Inc Form 483, 2013-04-02

FDA issued a Form 483 to Topix Pharmaceuticals Inc on 2013-04-02 with 4 public-safe observations.

483· Form 483 issuedHuman Drugs4 observations

Topix Pharmaceuticals Inc · Amityville, United States · Issued April 2, 2013

Overview

  • 4 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.

2 Apr 2013
21 CFR 211.46(b)

Equipment for Environmental Control

Cited by Charisse K Green

2 Apr 2013
21 CFR 211.100(a)

Approval and review of procedures

Cited by Charisse K Green

2 Apr 2013
21 CFR 211.100(b)

SOPs not followed / documented

Cited by Charisse K Green

2 Apr 2013
21 CFR 211.160(b)(4)

Calibration - at intervals, written program, remedial action

Cited by Charisse K Green

Inspected site

TPTopix Pharmaceuticals IncAmityville, United States

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 observations1x
21 CFR 211.100(b)Cited across public-safe Form 483 observations1x
21 CFR 211.160(b)(4)Cited across public-safe Form 483 observations1x
21 CFR 211.46(b)Cited across public-safe Form 483 observations1x

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 4 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