Interstate Blood Bank Inc Of Missouri FDA Inspection Record

FEI 1000115480 · Inspections, Form 483s, warning letters and import refusals

Interstate Blood Bank Inc Of Missouri is an FDA-inspected facility (FEI 1000115480) located in Muskegon, MI, US. RegDataLab tracks 4 FDA inspections at this facility.

What FDA found at this site

Latest inspection
Nov 1, 2019: No Action Indicated (NAI)
Inspections on record
4 (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
Recalls as the recalling firm
4, latest Jul 1, 2005

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
Nov 1, 2019No Action Indicated (NAI)No citations listed
Jun 30, 2017No Action Indicated (NAI)No citations listed
Apr 19, 2012No Action Indicated (NAI)No citations listed
Jun 2, 2010No Action Indicated (NAI)No citations listed

Recalls

Newest first. 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
Jul 1, 2005Class IIB-0058-6Source Plasma
Source Plasma, collected from an ineligible donor who had been permanently deferred due to drug use, was distributed.
May 18, 2005Class IIB-2125-5Source Plasma
Blood products, which were collected from a donor who had engaged in high risk behavior activities, were distributed.
Jan 30, 2004Class IIIB-1194-4Source Plasma
Blood products, which tested negative for infectious diseases by viral marker screening tests, but were collected from a donor in which…
Apr 28, 2003Class IIB-1469-3source plasma
Blood product, collected from a donor who had body piercing within twelve months of donation, was 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.

3 records behind this number
RecordDatePoints x age weightAdds
Class II recall B-0058-6, this FEI as the recalling firmJul 1, 200510 years or older, so it adds no points0
Class II recall B-2125-5, this FEI as the recalling firmMay 18, 200510 years or older, so it adds no points0
Class II recall B-1469-3, this FEI as the recalling firmApr 28, 200310 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
Muskegon, MI (US)
Source
inspections

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