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Interstate Blood Bank Inc Of Missouri FDA Inspection Record

FEI 1045035 · Inspections, Form 483s, warning letters and import refusals

Interstate Blood Bank Inc Of Missouri is an FDA-inspected facility (FEI 1045035) located in Knoxville, TN, US. RegDataLab tracks 5 FDA inspections at this facility.

What FDA found at this site

Latest inspection: Aug 28, 2019: No Action Indicated (NAI)
Inspections on record: 5 (5 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: 33, latest May 7, 2013

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.

Date	Result	What FDA cited
Aug 28, 2019	No Action Indicated (NAI)	No citations listed
Nov 9, 2016	No Action Indicated (NAI)	No citations listed
Jan 9, 2015	No Action Indicated (NAI)	No citations listed
Mar 2, 2012	No Action Indicated (NAI)	No citations listed
Nov 5, 2009	No Action Indicated (NAI)	No citations listed

Recalls

Showing the 10 most recent of 33 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.

Date	Class	Recall	Product and reason
May 7, 2013	Class II	B-2379-13	Source Plasma Blood products, collected from a donor who received a tattoo within 12 months of donation, were distributed.
Oct 26, 2012	Class II	B-0469-13	Source Plasma Blood product, collected from a donor with a history of incarceration, was distributed.
Sep 10, 2012	Class III	B-0160-13	Source Plasma Blood product, collected from a donor for whom donor suitability was not adequately determined, was distributed.
Apr 17, 2007	Class II	B-1944-08	Source Plasma Blood product, collected from a donor whose scheduled physical exam was overdue, was distributed.
Jan 18, 2006	Class III	B-0713-7	Source Plasma Blood product, collected from a donor who did not have a complete medical history interview, was distributed.
Aug 12, 2005	Class III	B-0750-7	Source Plasma Blood products, collected from a donor who did not have a complete medical history interview, were distributed.
Aug 10, 2005	Class III	B-0714-7	Source Plasma Blood products, collected from a donor who did not have a complete medical history interview, were distributed.
Aug 10, 2005	Class III	B-0715-7	Source Plasma Blood products, collected from a donor who did not have a complete medical history interview, were distributed.
Aug 9, 2005	Class III	B-0716-7	Source Plasma Blood products, collected from a donor who did not have a complete medical history interview, were distributed.
Aug 9, 2005	Class III	B-0717-7	Source Plasma Blood products, collected from a donor who did not have a complete medical history interview, were distributed.

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.

4 records behind this number

Record	Date	Points x age weight
Class II recall B-2379-13, this FEI as the recalling firm	May 7, 2013	10 years or older, so it adds no points
Class II recall B-0469-13, this FEI as the recalling firm	Oct 26, 2012	10 years or older, so it adds no points
Class II recall B-1944-08, this FEI as the recalling firm	Apr 17, 2007	10 years or older, so it adds no points
Class II recall B-1063-5, this FEI as the recalling firm	Mar 11, 2004	10 years or older, so it adds no points

When each source was last refreshed

FDA sources behind this page and when RegDataLab last refreshed each one
Records	Last refreshed	Source as of	Status
Inspections	Nov 15, 2026	Newest record Nov 5, 2026	Current
Inspection citations	Nov 15, 2026	Newest record Nov 5, 2026	Current
Compliance actions (warning letters, injunctions and other action types)	Nov 2, 2026	Newest record Oct 29, 2026	Current
Warning letter text	Nov 14, 2026	Newest record Nov 10, 2026	Current
Recalls (Enforcement Report)	Nov 15, 2026	Newest record Nov 11, 2026	Current
Form 483s and inspection documents	Nov 13, 2026	Newest record Nov 12, 2026	Current
Import refusals	Nov 15, 2026	Newest record Nov 5, 2026	Current

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Facility details

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