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New York Blood Center Enterprises FDA Inspection Record

FEI 3007075120 · Inspections, Form 483s, warning letters and import refusals

New York Blood Center Enterprises is an FDA-inspected facility (FEI 3007075120) located in Rockville Centre, NY, US. RegDataLab tracks 7 FDA inspections at this facility.

What FDA found at this site

Latest inspection
Jan 12, 2026: Voluntary Action Indicated (VAI)
Inspections on record
7 (3 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
Jan 12, 2026Voluntary Action Indicated (VAI)Required records (21 CFR 606.160(b))
Following manufacturer's instructions (21 CFR 606.65(e))
Establish, maintain and follow manufacturing SOPs (21 CFR 606.100(b))
Written SOPs available for use by personnel (21 CFR 606.100(b))
Aug 3, 2022Voluntary Action Indicated (VAI)Establish, maintain and follow manufacturing SOPs (21 CFR 606.100(b))
Jul 31, 2018No Action Indicated (NAI)No citations listed
Feb 16, 2016No Action Indicated (NAI)No citations listed
Apr 10, 2014No Action Indicated (NAI)No citations listed
Mar 29, 2012Voluntary Action Indicated (VAI)Provide space for examination (21 CFR 606.40(a)(1))
Establish, maintain and follow manufacturing SOPs (21 CFR 606.100(b))
Nov 24, 2009No Action Indicated (NAI)No citations listed

FDA record score

10 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.

3 records behind this number
RecordDatePoints x age weightAdds
Inspection classified VAIJan 12, 20266 x 16
Inspection classified VAIAug 3, 20226 x 0.63.6
Inspection classified VAIMar 29, 201210 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 14, 2026Newest record Nov 5, 2026Current
Inspection citationsNov 14, 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 14, 2026Newest record Nov 11, 2026Current
Form 483s and inspection documentsNov 13, 2026Newest record Nov 12, 2026Current
Import refusalsNov 2, 2026Newest record Oct 22, 2026Current

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Facility details

Company
New York Blood Center Enterprises
Location
Rockville Centre, NY (US)
Source
inspections

FDA data resources

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