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Pacific Reproductive Center, Inc. FDA Record

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

Pacific Reproductive Center, Inc. has 0 FDA recalls, 18 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Pacific Reproductive Center, Inc." is on file. FDA has published 1 Form 483 for Pacific Reproductive Center, Inc..

What these totals cover: FDA records filed under the name "Pacific Reproductive Center, Inc." and its spelling variant "Pacific Reproductive Center".

Latest inspection: Mar 12, 2025 · VAI

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	18	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

Pacific Reproductive Center, Inc.'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	2	0	0	0	0
2024	1	0	0	0	0
2023	1	0	0	0	0
2022	0	0	0	0	0
2021	0	0	0	0	0
2020	0	0	0	0	0
2019	2	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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Pacific Reproductive Center, Inc. Form 483s

1 Form 483 published by FDA.

Date	Document	FEI
Jan 13, 2025 · Document on fda.gov	483	3005488001

A Form 483 lists the observations FDA investigators made at the end of an inspection. FDA publishes some Form 483s in its reading room, and each date links to that document. Read the observations with the FDA 483 search.

Recent FDA inspections

18 inspections from Dec 4, 2008 to Mar 12, 2025.

Date	Site	Product	Classification	FEI
Mar 12, 2025	Corona, CA	Biologics	Voluntary Action Indicated (VAI)	3006397643
Jan 13, 2025	Torrance, CA	Biologics	Voluntary Action Indicated (VAI)	3005488001
Aug 19, 2024	Irvine, CA	Biologics	Voluntary Action Indicated (VAI)	3005861788
Aug 31, 2023	Irvine, CA	Biologics	Voluntary Action Indicated (VAI)	3005861788
Apr 3, 2019	Corona, CA	Biologics	No Action Indicated (NAI)	3006397643
Apr 2, 2019	Torrance, CA	Biologics	No Action Indicated (NAI)	3005488001
Feb 15, 2018	Irvine, CA	Biologics	Voluntary Action Indicated (VAI)	3005861788
Aug 15, 2016	Torrance, CA	Biologics	No Action Indicated (NAI)	3005488001
Aug 24, 2015	Corona, CA	Biologics	No Action Indicated (NAI)	3006397643
Jul 6, 2015	Irvine, CA	Biologics	Voluntary Action Indicated (VAI)	3005861788
Jun 3, 2013	Glendale, CA	Biologics	No Action Indicated (NAI)	3009201791
Dec 18, 2012	Irvine, CA	Biologics	No Action Indicated (NAI)	3005861788
May 3, 2011	Irvine, CA	Biologics	No Action Indicated (NAI)	3005861788
Apr 27, 2011	Torrance, CA	Biologics	No Action Indicated (NAI)	3005488001
Sep 16, 2009	Chino Hills, CA	Biologics	No Action Indicated (NAI)	3006397945
Sep 15, 2009	Glendale, CA	Biologics	No Action Indicated (NAI)	3004092752
Jun 25, 2009	Corona, CA	Biologics	No Action Indicated (NAI)	3006397643
Dec 4, 2008	Irvine, CA	Biologics	Voluntary Action Indicated (VAI)	3005861788

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

6 inspected sites, newest inspection first.

Facility	Location	Inspections	Latest
FEI 3006397643	Corona, CA	4	Mar 12, 2025
FEI 3005488001	Torrance, CA	4	Jan 13, 2025
FEI 3005861788	Irvine, CA	7	Aug 19, 2024
FEI 3009201791	Glendale, CA	1	Jun 3, 2013
FEI 3006397945	Chino Hills, CA	1	Sep 16, 2009
FEI 3004092752	Glendale, CA	1	Sep 15, 2009

Pacific Reproductive Center, Inc. and the FDA: common questions

Has Pacific Reproductive Center, Inc. received an FDA warning letter?

No FDA warning letter addressed to the name "Pacific Reproductive Center, Inc." 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 Pacific Reproductive Center, Inc. received an FDA Form 483?

FDA has published 1 Form 483 for Pacific Reproductive Center, Inc. in its reading room, the most recent dated Jan 13, 2025. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect Pacific Reproductive Center, Inc.?

The most recent FDA inspection on file ended Mar 12, 2025 at Corona, CA and was classified VAI. FDA has 18 inspections of Pacific Reproductive Center, Inc. on file.

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