Form 483

Becton, Dickinson and Company, BD Biosciences Form 483, 2016-05-12

FDA issued a Form 483 to Becton, Dickinson and Company, BD Biosciences on 2016-05-12 with 9 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health9 observations

Becton, Dickinson and Company, BD Biosciences · San Jose, United States · Issued May 12, 2016

Overview

  • 9 public-safe observations are available for this inspection.
  • 3 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.

12 May 2016
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by Mary R Hole, Jacqueline M Cleary

12 May 2016
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by Mary R Hole, Jacqueline M Cleary

12 May 2016
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by Mary R Hole, Jacqueline M Cleary

12 May 2016
21 CFR 820.198(b)

Review and evaluation for investigation

Cited by Mary R Hole, Jacqueline M Cleary

12 May 2016
21 CFR 820.198(b)

Review and evaluation for investigation

Cited by Mary R Hole, Jacqueline M Cleary

Inspected site

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.198(a)Cited across public-safe Form 483 observations3x
21 CFR 820.198(b)Cited across public-safe Form 483 observations3x
21 CFR 820.75(a)Cited across public-safe Form 483 observations3x

Full 483 report

Get the verbatim text of all 9 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