Huntington Reproductive Center Medical Group FDA Record

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

  • Latest inspection VAI · Oct 29, 2024
  • No warning letters matched by name
Inspections 22 0 OAI
Recalls 0 0 Class I
Warning letters 0 None on file
510(k) clearances 0 None on file

Huntington Reproductive Center Medical Group has 0 FDA recalls, 22 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Huntington Reproductive Center Medical Group" is on file.

What these totals cover: FDA records filed under the name "Huntington Reproductive Center Medical Group".

Latest inspection
Oct 29, 2024 · VAI

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
Inspections22Nov 15, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

FDA record by year

Huntington Reproductive Center Medical Group's FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

Huntington Reproductive Center Medical Group: FDA inspections per year

YearInspectionsOAIWarning lettersRecall recordsClass I
202600000
202500000
202410000
202330000
202200000
202100000
202010000
201900000
201840000
201710000

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.

Reviewing Huntington Reproductive Center Medical Group as a supplier? Request a free FDA snapshot: name up to five suppliers and get a PDF of their public FDA record, with sources and dates. You do not need an API connection. Each snapshot is prepared by hand.

Check this supplier

Or check Huntington Reproductive Center Medical Group yourself in Claude, Cursor or ChatGPT: get the full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site.

Get a free API key

Recent FDA inspections

22 inspections from Jan 27, 2010 to Oct 29, 2024. Showing the 20 most recent. View all 22 inspections

DateSiteProductClassificationFEI
Oct 29, 2024Newport Beach, CABiologicsVoluntary Action Indicated (VAI)3009565053
Nov 6, 2023Pasadena, CABiologicsVoluntary Action Indicated (VAI)3003253380
Jun 1, 2023Los Angeles, CABiologicsNo Action Indicated (NAI)3006501046
Mar 28, 2023Newport Beach, CABiologicsNo Action Indicated (NAI)3009565053
Jan 8, 2020Fullerton, CABiologicsNo Action Indicated (NAI)3006501029
Dec 6, 2018Pasadena, CABiologicsVoluntary Action Indicated (VAI)3003253380
Apr 26, 2018Westlake Village, CABiologicsVoluntary Action Indicated (VAI)3005108085
Mar 23, 2018Newport Beach, CABiologicsNo Action Indicated (NAI)3009565053
Jan 19, 2018Los Angeles, CABiologicsNo Action Indicated (NAI)3006501046
Jul 14, 2017Fullerton, CABiologicsNo Action Indicated (NAI)3006501029
Sep 16, 2016Pasadena, CABiologicsNo Action Indicated (NAI)3003253380
Feb 2, 2016Los Angeles, CABiologicsNo Action Indicated (NAI)3006501046
Sep 9, 2015Newport Beach, CABiologicsNo Action Indicated (NAI)3009565053
Feb 5, 2015Westlake Village, CABiologicsVoluntary Action Indicated (VAI)3005108085
Sep 3, 2014Fullerton, CABiologicsNo Action Indicated (NAI)3006501029
Jan 10, 2013Pasadena, CABiologicsNo Action Indicated (NAI)3003253380
Nov 8, 2012Los Angeles, CABiologicsNo Action Indicated (NAI)3006501046
Dec 22, 2011Westlake Village, CABiologicsNo Action Indicated (NAI)3005108085
May 25, 2011Los Angeles, CABiologicsVoluntary Action Indicated (VAI)3006501046
May 18, 2011Fullerton, CABiologicsNo Action Indicated (NAI)3006501029
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

5 inspected sites, newest inspection first.

FacilityLocationInspectionsLatest
FEI 3009565053Newport Beach, CA4Oct 29, 2024
FEI 3003253380Pasadena, CA5Nov 6, 2023
FEI 3006501046Los Angeles, CA5Jun 1, 2023
FEI 3006501029Fullerton, CA4Jan 8, 2020
FEI 3005108085Westlake Village, CA4Apr 26, 2018

Huntington Reproductive Center Medical Group and the FDA: common questions

Has Huntington Reproductive Center Medical Group received an FDA warning letter?

No FDA warning letter addressed to the name "Huntington Reproductive Center Medical Group" 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 Huntington Reproductive Center Medical Group received an FDA Form 483?

FDA has not published a Form 483 for "Huntington Reproductive Center Medical Group" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect Huntington Reproductive Center Medical Group?

The most recent FDA inspection on file ended Oct 29, 2024 at Newport Beach, CA and was classified VAI. FDA has 22 inspections of Huntington Reproductive Center Medical Group on file.

Need more than this page shows? Ask about Huntington Reproductive Center Medical Group in Claude or ChatGPT and get every site's inspections, Form 483s, warning letters and import alerts, with a link to the FDA source for each record. The API key is free: no card.

Get a free API key

Prefer a PDF? Request a free supplier snapshot.

Is this your company or a supplier you list? Link to this FDA record from your site with a free button.

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