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Octapharma Plasma, Inc. Portsmouth FDA Record

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

Latest inspection NAI · Mar 30, 2021
No warning letters matched by name

Inspections 5

0 OAI

Recalls 0 0 Class I

Warning letters 0 None on file

510(k) clearances 0 None on file

Octapharma Plasma, Inc. Portsmouth has 0 FDA recalls, 5 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Octapharma Plasma, Inc. Portsmouth" is on file.

What these totals cover: FDA records filed under the name "Octapharma Plasma, Inc. Portsmouth".

Latest inspection: Mar 30, 2021 · 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	5	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

Octapharma Plasma, Inc. Portsmouth's FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

Octapharma Plasma, Inc. Portsmouth: FDA inspections per year

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

5 inspections from Jun 28, 2011 to Mar 30, 2021.

Date	Site	Product	Classification	FEI
Mar 30, 2021	Portsmouth, VA	Biologics	No Action Indicated (NAI)	3007166600
Sep 26, 2018	Portsmouth, VA	Biologics	Voluntary Action Indicated (VAI)	3007166600
Oct 28, 2016	Portsmouth, VA	Biologics	Voluntary Action Indicated (VAI)	3007166600
Jun 20, 2013	Portsmouth, VA	Biologics	No Action Indicated (NAI)	3007166600
Jun 28, 2011	Portsmouth, VA	Biologics	Voluntary Action Indicated (VAI)	3007166600

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 3007166600	Portsmouth, VA	5	Mar 30, 2021

Octapharma Plasma, Inc. Portsmouth and the FDA: common questions

Has Octapharma Plasma, Inc. Portsmouth received an FDA warning letter?

No FDA warning letter addressed to the name "Octapharma Plasma, Inc. Portsmouth" 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 Octapharma Plasma, Inc. Portsmouth received an FDA Form 483?

FDA has not published a Form 483 for "Octapharma Plasma, Inc. Portsmouth" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect Octapharma Plasma, Inc. Portsmouth?

The most recent FDA inspection on file ended Mar 30, 2021 at Portsmouth, VA and was classified NAI. FDA has 5 inspections of Octapharma Plasma, Inc. Portsmouth on file.

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