Form 483

Thorn BioScience Form 483, 2010-05-06

FDA issued a Form 483 to Thorn BioScience on 2010-05-06 with 4 public-safe observations.

483· Form 483 issued4 observations

Thorn BioScience · Louisville, United States · Issued May 6, 2010

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.

6 May 2010
21 CFR 211.113(b)

Validation lacking for sterile drug products

Cited by Kathleen D Culver

6 May 2010
21 CFR 211.182

Specific information required in individual logs

Cited by Kathleen D Culver

6 May 2010
21 CFR 211.188(b)(3)

Identification of each component or in-process material

Cited by Kathleen D Culver

6 May 2010
21 CFR 211.194(e)

Stability testing records not included

Cited by Kathleen D Culver

Inspected site

TBThorn BioScienceLouisville, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.113(b)Cited across public-safe Form 483 observations1x
21 CFR 211.182Cited across public-safe Form 483 observations1x
21 CFR 211.188(b)(3)Cited across public-safe Form 483 observations1x
21 CFR 211.194(e)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 4 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