Form 483

Agnitio Inc Form 483, 2018-11-09

FDA issued a Form 483 to Agnitio Inc on 2018-11-09 with 12 public-safe observations.

483· Form 483 issuedHuman Drugs12 observations

Agnitio Inc · Appleton, United States · Issued November 9, 2018

Overview

  • 12 public-safe observations are available for this inspection.
  • 6 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.

9 Nov 2018
21 CFR 211.113(a)

Procedures for non-sterile drug products

Cited by Sandra A Hughes, Sandra A Boyd

9 Nov 2018
21 CFR 211.165(c)

Sampling and testing plans not described

Cited by Sandra A Hughes, Sandra A Boyd

9 Nov 2018
21 CFR 211.166(a)(3)

Valid stability test methods

Cited by Sandra A Hughes, Sandra A Boyd

9 Nov 2018
21 CFR 211.192

Investigations of discrepancies, failures

Cited by Sandra A Hughes, Sandra A Boyd

9 Nov 2018
21 CFR 211.22(d)

Procedures not in writing, fully followed

Cited by Sandra A Hughes, Sandra A Boyd

Inspected site

AIAgnitio IncAppleton, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.113(a)Cited across public-safe Form 483 observations2x
21 CFR 211.165(c)Cited across public-safe Form 483 observations2x
21 CFR 211.166(a)(3)Cited across public-safe Form 483 observations2x
21 CFR 211.192Cited across public-safe Form 483 observations2x
21 CFR 211.22(d)Cited across public-safe Form 483 observations2x
21 CFR 211.67(b)Cited across public-safe Form 483 observations2x

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 12 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