Form 483

New York Blood Center Enterprises Form 483, 2011-08-02

FDA issued a Form 483 to New York Blood Center Enterprises on 2011-08-02 with 5 public-safe observations.

483· Form 483 issued5 observations

New York Blood Center Enterprises · Rye, United States · Issued August 2, 2011

Overview

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

2 Aug 2011
21 CFR 211.100(a)

Changes to Procedures Not Reviewed, Approved

Cited by Evelyn Taha, Matthew R Palo

2 Aug 2011
21 CFR 211.100(b)

SOPs not followed / documented

Cited by Evelyn Taha, Matthew R Palo

2 Aug 2011
21 CFR 211.160(b)

Scientifically sound laboratory controls

Cited by Evelyn Taha, Matthew R Palo

2 Aug 2011
21 CFR 606.100(c)

Thorough investigations

Cited by Evelyn Taha, Matthew R Palo

2 Aug 2011
21 CFR 606.171

Biological product deviation report

Cited by Evelyn Taha, Matthew R Palo

Inspected site

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.100(a)Cited across public-safe Form 483 observations1x
21 CFR 211.100(b)Cited across public-safe Form 483 observations1x
21 CFR 211.160(b)Cited across public-safe Form 483 observations1x
21 CFR 606.100(c)Cited across public-safe Form 483 observations1x
21 CFR 606.171Cited 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