Form 483

The American National Red Cross Diagnostic Manufacturing Division Form 483, 2011-11-04

FDA issued a Form 483 to The American National Red Cross Diagnostic Manufacturing Division on 2011-11-04 with 5 public-safe observations.

483· Form 483 issued5 observations

The American National Red Cross Diagnostic Manufacturing Division · Gaithersburg, United States · Issued November 4, 2011

Overview

  • 5 public-safe observations are available for this inspection.
  • 5 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.

4 Nov 2011
21 CFR 601.12(c)

Moderate changes to an approved application

Cited by Helen B Ricalde

4 Nov 2011
21 CFR 601.12(d)

Minor changes to an approved application

Cited by Helen B Ricalde

4 Nov 2011
21 CFR 820.50

Purchasing controls, Lack of or inadequate procedures

Cited by Helen B Ricalde

4 Nov 2011
21 CFR 820.90(a)

Specific non-conforming product procedures

Cited by Helen B Ricalde

4 Nov 2011
21 CFR 820.100(a)(3)

Identification of actions needed

Cited by Helen B Ricalde

Inspected site

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 601.12(c)Cited across public-safe Form 483 observations1x
21 CFR 601.12(d)Cited across public-safe Form 483 observations1x
21 CFR 820.100(a)(3)Cited across public-safe Form 483 observations1x
21 CFR 820.50Cited across public-safe Form 483 observations1x
21 CFR 820.90(a)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 5 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