Form 483

Specialty Blood Center Form 483, 2011-02-10

FDA issued a Form 483 to Specialty Blood Center on 2011-02-10 with 7 public-safe observations.

483· Form 483 issued7 observations

Specialty Blood Center · Charleston, United States · Issued February 10, 2011

Overview

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

10 Feb 2011
21 CFR 606.40(d)(2)

Provide adequate disposal of blood & blood components

Cited by Brandy Davis Brown

10 Feb 2011
21 CFR 606.60(a)

Equipment observed, standardized, calibrated

Cited by Brandy Davis Brown

10 Feb 2011
21 CFR 606.100(b)

Establish, maintain and follow manufacturing SOPs

Cited by Brandy Davis Brown

10 Feb 2011
21 CFR 606.100(c)

Record review prior to release

Cited by Brandy Davis Brown

10 Feb 2011
21 CFR 606.100(c)

Thorough investigations

Cited by Brandy Davis Brown

Inspected site

SBSpecialty Blood CenterCharleston, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 606.100(c)Cited across public-safe Form 483 observations2x
21 CFR 606.100(b)Cited across public-safe Form 483 observations1x
21 CFR 606.160(a)(1)Cited across public-safe Form 483 observations1x
21 CFR 606.160(b)Cited across public-safe Form 483 observations1x
21 CFR 606.40(d)(2)Cited across public-safe Form 483 observations1x
21 CFR 606.60(a)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 7 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