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Coastal Bend Blood Center FDA Record

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

Coastal Bend Blood Center has 0 FDA recalls, 7 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Coastal Bend Blood Center" is on file.

What these totals cover: FDA records filed under the name "Coastal Bend Blood Center".

Latest inspection: Mar 28, 2025 · NAI

Summary

Record counts and when each FDA source was last refreshed
Records	Count	Last refreshed	Source as of	Status
Recalls	0	Nov 8, 2026	File dated Nov 3, 2026	Current
510(k) clearances	0	Nov 8, 2026	File dated Nov 2, 2026	Current
Inspections	7	Nov 14, 2026	Newest record Nov 5, 2026	Current
Compliance actions	0	Nov 2, 2026	Newest record Oct 29, 2026	Current

FDA record by year

Coastal Bend Blood Center's FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

Year	Inspections	OAI	Warning letters	Recall records	Class I
2026	0	0	0	0	0
2025	1	0	0	0	0
2024	0	0	0	0	0
2023	0	0	0	0	0
2022	0	0	0	0	0
2021	0	0	0	0	0
2020	0	0	0	0	0
2019	1	0	0	0	0
2018	0	0	0	0	0
2017	1	0	0	0	0

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

7 inspections from Jun 8, 2009 to Mar 28, 2025.

Date	Site	Product	Classification	FEI
Mar 28, 2025	Corpus Christi, TX	Biologics	No Action Indicated (NAI)	1671283
Jun 13, 2019	Corpus Christi, TX	Biologics	No Action Indicated (NAI)	1671283
Jul 14, 2017	Corpus Christi, TX	Biologics	Voluntary Action Indicated (VAI)	1671283
Jun 17, 2015	Corpus Christi, TX	Biologics	No Action Indicated (NAI)	1671283
Apr 12, 2013	Corpus Christi, TX	Biologics	No Action Indicated (NAI)	1671283
Jun 15, 2011	Corpus Christi, TX	Biologics	No Action Indicated (NAI)	1671283
Jun 8, 2009	Corpus Christi, TX	Biologics	Voluntary Action Indicated (VAI)	1671283

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

1 inspected site, newest inspection first.

Facility	Location	Inspections	Latest
FEI 1671283	Corpus Christi, TX	7	Mar 28, 2025

Coastal Bend Blood Center and the FDA: common questions

Has Coastal Bend Blood Center received an FDA warning letter?

No FDA warning letter addressed to the name "Coastal Bend Blood Center" 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 Coastal Bend Blood Center received an FDA Form 483?

FDA has not published a Form 483 for "Coastal Bend Blood Center" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect Coastal Bend Blood Center?

The most recent FDA inspection on file ended Mar 28, 2025 at Corpus Christi, TX and was classified NAI. FDA has 7 inspections of Coastal Bend Blood Center on file.

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