Form 483

Septodont Inc. Form 483, 2011-08-25

FDA issued a Form 483 to Septodont Inc. on 2011-08-25 with 8 public-safe observations.

483· Form 483 issued8 observations

Septodont Inc. · Louisville, United States · Issued August 25, 2011

Overview

  • 8 public-safe observations are available for this inspection.
  • 7 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.

25 Aug 2011
21 CFR 211.22(a)

Authority lacking to review records, investigate errors

Cited by Erika V Butler

25 Aug 2011
21 CFR 211.22(a)

Lack of quality control unit

Cited by Erika V Butler

25 Aug 2011
21 CFR 211.25(a)

GMP Training Frequency

Cited by Erika V Butler

25 Aug 2011
21 CFR 211.80(a)

Procedures To Be in Writing

Cited by Erika V Butler

25 Aug 2011
21 CFR 211.100(b)

SOPs not followed / documented

Cited by Erika V Butler

Inspected site

SISeptodont Inc.Louisville, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.22(a)Cited across public-safe Form 483 observations2x
21 CFR 211.100(b)Cited across public-safe Form 483 observations1x
21 CFR 211.101(d)Cited across public-safe Form 483 observations1x
21 CFR 211.105(b)Cited across public-safe Form 483 observations1x
21 CFR 211.170(b)Cited across public-safe Form 483 observations1x
21 CFR 211.25(a)Cited across public-safe Form 483 observations1x
21 CFR 211.80(a)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 8 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