Kaiser Permanente Center For Reproductive Health FDA Record

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

  • Latest inspection NAI · Sep 18, 2026
  • No warning letters matched by name
Inspections 11 0 OAI
Recalls 0 0 Class I
Warning letters 0 None on file
510(k) clearances 0 None on file

Kaiser Permanente Center For Reproductive Health has 0 FDA recalls, 11 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Kaiser Permanente Center For Reproductive Health" is on file.

What these totals cover: FDA records filed under the name "Kaiser Permanente Center For Reproductive Health".

Latest inspection
Sep 18, 2026 · 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
Inspections11Nov 15, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

FDA record by year

Kaiser Permanente Center For Reproductive Health's FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

Kaiser Permanente Center For Reproductive Health: FDA inspections per year

YearInspectionsOAIWarning lettersRecall recordsClass I
202610000
202510000
202400000
202300000
202200000
202110000
202000000
201910000
201800000
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.

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Recent FDA inspections

11 inspections from May 2, 2011 to Sep 18, 2026.

DateSiteProductClassificationFEI
Sep 18, 2026Fremont, CABiologicsNo Action Indicated (NAI)3004740553
Aug 7, 2025Sacramento, CABiologicsNo Action Indicated (NAI)3006304159
Nov 17, 2021Sacramento, CABiologicsNo Action Indicated (NAI)3006304159
Sep 12, 2019Fremont, CABiologicsNo Action Indicated (NAI)3004740553
Jul 11, 2017Sacramento, CABiologicsNo Action Indicated (NAI)3006304159
Aug 17, 2016Fremont, CABiologicsNo Action Indicated (NAI)3004740553
Dec 18, 2014Sacramento, CABiologicsNo Action Indicated (NAI)3006304159
Oct 29, 2013Fremont, CABiologicsNo Action Indicated (NAI)3004740553
Jun 27, 2013Sacramento, CABiologicsNo Action Indicated (NAI)3006304159
Oct 26, 2011Fremont, CABiologicsNo Action Indicated (NAI)3004740553
May 2, 2011Sacramento, CABiologicsNo Action Indicated (NAI)3006304159
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

2 inspected sites, newest inspection first.

FacilityLocationInspectionsLatest
FEI 3004740553Fremont, CA5Sep 18, 2026
FEI 3006304159Sacramento, CA6Aug 7, 2025

Kaiser Permanente Center For Reproductive Health and the FDA: common questions

Has Kaiser Permanente Center For Reproductive Health received an FDA warning letter?

No FDA warning letter addressed to the name "Kaiser Permanente Center For Reproductive Health" 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 Kaiser Permanente Center For Reproductive Health received an FDA Form 483?

FDA has not published a Form 483 for "Kaiser Permanente Center For Reproductive Health" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect Kaiser Permanente Center For Reproductive Health?

The most recent FDA inspection on file ended Sep 18, 2026 at Fremont, CA and was classified NAI. FDA has 11 inspections of Kaiser Permanente Center For Reproductive Health on file.

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