Community Blood Center Of Greater Kansas City FDA Record

Warning letters, Form 483s, inspections, recalls and 510(k) clearances

  • Latest inspection NAI · Dec 9, 2025
  • No warning letters matched by name
Inspections 35 0 OAI
Recalls 0 0 Class I
Warning letters 0 None on file
510(k) clearances 0 None on file

Community Blood Center Of Greater Kansas City has 0 FDA recalls, 35 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Community Blood Center Of Greater Kansas City" is on file.

What these totals cover: FDA records filed under the name "Community Blood Center Of Greater Kansas City".

Latest inspection
Dec 9, 2025 · NAI

Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 11, 2026 (checked Nov 15, 2026, unchanged)File dated Nov 10, 2026Current
510(k) clearances0Nov 15, 2026File dated Nov 9, 2026Current
Inspections35Nov 15, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

FDA record by year

Community Blood Center Of Greater Kansas City's FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

Community Blood Center Of Greater Kansas City: FDA inspections per year

YearInspectionsOAIWarning lettersRecall recordsClass I
202600000
202520000
202400000
202310000
202210000
202100000
202010000
201910000
201820000
201700000

Inspections are counted by the date they ended, warning letters by the date FDA issued them and recall records by the recall start date. FDA lists one recall record per recalled product, so one recall event can add several.

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Recent FDA inspections

35 inspections from Oct 23, 2008 to Dec 9, 2025. Showing the 20 most recent. View all 35 inspections

DateSiteProductClassificationFEI
Dec 9, 2025Saint Joseph, MOBiologicsNo Action Indicated (NAI)1978038
Mar 7, 2025Kansas City, MOBiologicsNo Action Indicated (NAI)1972933
Nov 14, 2023Overland Park, KSBiologicsNo Action Indicated (NAI)1000511013
Sep 27, 2022Kansas City, MOBiologicsNo Action Indicated (NAI)1972933
Mar 11, 2020Saint Joseph, MOBiologicsNo Action Indicated (NAI)1978038
Jan 25, 2019Overland Park, KSBiologicsNo Action Indicated (NAI)1000511013
Jul 5, 2018Saint Joseph, MOBiologicsNo Action Indicated (NAI)1978038
Apr 6, 2018Kansas City, MOBiologicsNo Action Indicated (NAI)1972933
Oct 26, 2016Overland Park, KSBiologicsNo Action Indicated (NAI)1000511013
Dec 1, 2015Saint Joseph, MOBiologicsNo Action Indicated (NAI)1978038
Jan 22, 2015Overland Park, KSBiologicsNo Action Indicated (NAI)1000511013
Oct 16, 2014Kansas City, MODevicesNo Action Indicated (NAI)1972933
Dec 13, 2013Saint Joseph, MOBiologicsVoluntary Action Indicated (VAI)1978038
Jun 12, 2013Overland Park, KSBiologicsNo Action Indicated (NAI)1000511013
Mar 15, 2013Saint Joseph, MOBiologicsVoluntary Action Indicated (VAI)1978038
Nov 7, 2012Kansas City, MOBiologicsVoluntary Action Indicated (VAI)1972933
Nov 7, 2012Kansas City, MOBiologicsNo Action Indicated (NAI)3006853984
Feb 28, 2012Columbia, MOBiologicsNo Action Indicated (NAI)3004461077
Nov 4, 2011Kansas City, MOBiologicsVoluntary Action Indicated (VAI)1972933
Nov 4, 2011Kansas City, MOBiologicsNo Action Indicated (NAI)3006853984
NAI
No objectionable conditions or practices were found during the inspection.
VAI
Objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.
OAI
Regulatory and/or administrative actions are recommended.

Look up the inspector observations behind these results with the FDA 483 search, or check for formal enforcement with the FDA warning letter search.

FDA-inspected facilities

7 inspected sites, newest inspection first.

FacilityLocationInspectionsLatest
FEI 1978038Saint Joseph, MO8Dec 9, 2025
FEI 1972933Kansas City, MO10Mar 7, 2025
FEI 1000511013Overland Park, KS8Nov 14, 2023
FEI 3006853984Kansas City, MO4Nov 7, 2012
FEI 3004461077Columbia, MO2Feb 28, 2012
FEI 3004853541Olathe, KS2Oct 14, 2011
FEI 3000202881Lawrence, KS1May 15, 2009

Community Blood Center Of Greater Kansas City and the FDA: common questions

Has Community Blood Center Of Greater Kansas City received an FDA warning letter?

No FDA warning letter addressed to the name "Community Blood Center Of Greater Kansas City" is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.

Has Community Blood Center Of Greater Kansas City received an FDA Form 483?

FDA has not published a Form 483 for "Community Blood Center Of Greater Kansas City" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect Community Blood Center Of Greater Kansas City?

The most recent FDA inspection on file ended Dec 9, 2025 at Saint Joseph, MO and was classified NAI. FDA has 35 inspections of Community Blood Center Of Greater Kansas City on file.

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