Form 483

Rhode Island Blood Center, A Division of New York Blood Center, Inc. Form 483, 2014-08-20

FDA issued a Form 483 to Rhode Island Blood Center, A Division of New York Blood Center, Inc. on 2014-08-20 with 5 public-safe observations.

483· Form 483 issuedBiologics5 observations

Rhode Island Blood Center, A Division of New York Blood Center, Inc. · Providence, United States · Issued August 20, 2014

Overview

  • 5 public-safe observations are available for this inspection.
  • 4 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.

20 Aug 2014
21 CFR 600.14(c)

When to report

Cited by Lorayne A Mcguinness, Alice C Silva

20 Aug 2014
21 CFR 606.100(b)

Establish, maintain and follow manufacturing SOPs

Cited by Lorayne A Mcguinness, Alice C Silva

20 Aug 2014
21 CFR 606.160(a)(1)

Concurrent documentation

Cited by Lorayne A Mcguinness, Alice C Silva

20 Aug 2014
21 CFR 606.160(a)(1)

Person performing, test results, interpretation

Cited by Lorayne A Mcguinness, Alice C Silva

20 Aug 2014
21 CFR 606.160(b)

Required records

Cited by Lorayne A Mcguinness, Alice C Silva

Inspected site

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 606.160(a)(1)Cited across public-safe Form 483 observations2x
21 CFR 600.14(c)Cited across public-safe Form 483 observations1x
21 CFR 606.100(b)Cited across public-safe Form 483 observations1x
21 CFR 606.160(b)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