Form 483

Rhode Island Blood Center, A Division of New York Blood Center, Inc. Form 483, 2025-08-01

FDA issued a Form 483 to Rhode Island Blood Center, A Division of New York Blood Center, Inc. on 2025-08-01 with 3 public-safe observations.

483· Form 483 issuedBiologics3 observations

Rhode Island Blood Center, A Division of New York Blood Center, Inc. · Providence, United States · Issued August 1, 2025

Overview

  • 3 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.

1 Aug 2025
21 CFR 606.100(b)

Establish, maintain and follow manufacturing SOPs

Cited by Amy Kim, Amy W Yan-Mai

1 Aug 2025
21 CFR 606.160(a)(1)

Person performing, test results, interpretation

Cited by Amy Kim, Amy W Yan-Mai

1 Aug 2025
21 CFR 606.65

Safe, sanitary, orderly storage

Cited by Amy Kim, Amy W Yan-Mai

Inspected site

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
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 606.65Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 3 observations

The full inspection record, as Atlas holds it, 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