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Interstate Blood Bank Inc Of Missouri FDA Inspection Record

FEI 3002660757 · Inspections, Form 483s, warning letters and import refusals

Interstate Blood Bank Inc Of Missouri is an FDA-inspected facility (FEI 3002660757) located in Jackson, TN, US. RegDataLab tracks 3 FDA inspections at this facility.

What FDA found at this site

Latest inspection
Jan 30, 2020: No Action Indicated (NAI)
Inspections on record
3 (1 VAI, 2 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
Recalls as the recalling firm
21, latest Feb 15, 2008

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 30, 2020No Action Indicated (NAI)No citations listed
Jan 20, 2017No Action Indicated (NAI)No citations listed
Feb 16, 2011Voluntary Action Indicated (VAI)Adverse Reaction- Reports of Investigations (21 CFR 606.170(a))
Establish, maintain and follow manufacturing SOPs (21 CFR 606.100(b))
Donor qualifying tests & measurements (21 CFR 606.100(b)(2))

Recalls

Showing the 10 most recent of 21 recalls. Recalls FDA's Enforcement Report lists with this FEI as the recalling firm. The recalling firm is not always the site that made the product. Search FDA's Enforcement Report by recall number.

DateClassRecallProduct and reason
Feb 15, 2008Class IIIB-1954-08Source Plasma
Blood product, collected from a donor whose suitability to donate was not adequately determined, was distributed.
Feb 15, 2008Class IIIB-1959-08Source Plasma
Blood product, collected from a donor whose suitability to donate was not adequately determined, was distributed.
Feb 15, 2008Class IIIB-2003-08Source Plasma
Blood product, collected from a donor whose suitability to donate was not adequately determined, was distributed.
Feb 15, 2008Class IIIB-2010-08Source Plasma
Blood product, which was collected from a donor in which donor suitability was not adequately determined, was distributed.
Feb 5, 2008Class IIIB-1960-08Source Plasma
Blood product, collected from a donor whose suitability to donate was not adequately determined, was distributed.
Feb 5, 2008Class IIIB-2004-08Source Plasma
Blood product, collected from a donor whose suitability to donate was not adequately determined, was distributed.
Feb 4, 2008Class IIIB-1958-08Source Plasma
Blood product, collected from a donor whose suitability to donate was not adequately determined, was distributed.
Aug 14, 2007Class IIB-1366-08Source Plasma
Blood products, collected from a donor who was deferred for a history of incarceration, were distributed.
May 28, 2004Class IIB-1349-5Source Plasma
Blood products, that tested negative for viral markers, but were not properly quarantined after the receipt of deferral information related…
Nov 7, 2003Class IIIB-1265-5Source Plasma
Blood products, collected from a donor that was not properly asked the medical history questions, including those questions concerning…

FDA record score

0 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.

7 records behind this number
RecordDatePoints x age weightAdds
Inspection classified VAIFeb 16, 201110 years or older, so it adds no points0
Class II recall B-1366-08, this FEI as the recalling firmAug 14, 200710 years or older, so it adds no points0
Class II recall B-1349-5, this FEI as the recalling firmMay 28, 200410 years or older, so it adds no points0
Class II recall B-1301-5, this FEI as the recalling firmJul 21, 200310 years or older, so it adds no points0
Class II recall B-1748-3, this FEI as the recalling firmJan 16, 200310 years or older, so it adds no points0
Class II recall B-1749-3, this FEI as the recalling firmAug 28, 200110 years or older, so it adds no points0
Class II recall B-1747-3, this FEI as the recalling firmJan 16, 200110 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

Company
Interstate Blood Bank Inc Of Missouri
Location
Jackson, TN (US)
Source
inspections

FDA data resources

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