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Rhode Island Blood Center, A Division Of New York Blood Center, Inc. Woonsocket Donor Center FDA Inspection Record

FEI 3005078114 · Inspections, Form 483s, warning letters and import refusals

Rhode Island Blood Center, A Division Of New York Blood Center, Inc. Woonsocket Donor Center is an FDA-inspected facility (FEI 3005078114) located in Woonsocket, RI, US. RegDataLab tracks 8 FDA inspections at this facility.

What FDA found at this site

Latest inspection
Apr 21, 2026: No Action Indicated (NAI)
Inspections on record
8 (4 VAI, 4 NAI)
Last OAI inspection
None on record
Warning letters
None matched to this FEI. Many letters do not state an FEI: search warning letters by company name

A Form 483 lists an inspector's observations. OAI means FDA recommends regulatory and/or administrative action. A warning letter is FDA's formal enforcement notice. No record here does not establish that a site is safe. Check this site on FDA's Data Dashboard.

Inspections and what FDA cited

Newest first. Citations are the inspector observations FDA publishes for the inspection.

DateResultWhat FDA cited
Apr 21, 2026No Action Indicated (NAI)No citations listed
Dec 9, 2021No Action Indicated (NAI)No citations listed
Dec 4, 2018No Action Indicated (NAI)No citations listed
Mar 9, 2017Voluntary Action Indicated (VAI)Establish, maintain and follow manufacturing SOPs (21 CFR 606.100(b))
Feb 26, 2015No Action Indicated (NAI)No citations listed
Mar 8, 2013Voluntary Action Indicated (VAI)No citations listed
Oct 28, 2011Voluntary Action Indicated (VAI)Required records (21 CFR 606.160(b))
Establish, maintain and follow manufacturing SOPs (21 CFR 606.100(b))
Donor notification (21 CFR 606.100(b)(21))
Aug 5, 2010Voluntary Action Indicated (VAI)Items to cover on annual reviews (21 CFR 211.180(e)(2))

FDA record score

2 of 100. A count of this site's adverse public FDA records, weighted by how recent each one is. A higher number means more, or more recent, records. Each record below adds the points shown.

Counted on Nov 15, 2026, method version 1. It counts records and does not judge the site: a low number does not establish that a site is safe, and sites that FDA inspects more often can collect more points. How this is counted.

4 records behind this number
RecordDatePoints x age weightAdds
Inspection classified VAIMar 9, 20176 x 0.251.5
Inspection classified VAIMar 8, 201310 years or older, so it adds no points0
Inspection classified VAIOct 28, 201110 years or older, so it adds no points0
Inspection classified VAIAug 5, 201010 years or older, so it adds no points0

When each source was last refreshed

FDA sources behind this page and when RegDataLab last refreshed each one
RecordsLast refreshedSource as ofStatus
InspectionsNov 15, 2026Newest record Nov 5, 2026Current
Inspection citationsNov 15, 2026Newest record Nov 5, 2026Current
Compliance actions (warning letters, injunctions and other action types)Nov 2, 2026Newest record Oct 29, 2026Current
Warning letter textNov 14, 2026Newest record Nov 10, 2026Current
Recalls (Enforcement Report)Nov 15, 2026Newest record Nov 11, 2026Current
Form 483s and inspection documentsNov 13, 2026Newest record Nov 12, 2026Current
Import refusalsNov 15, 2026Newest record Nov 5, 2026Current

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Facility details

Location
Woonsocket, RI (US)
Source
inspections

FDA data resources

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.