Los Angeles IVF Laboratory FDA Record

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

Los Angeles IVF Laboratory has 0 FDA recalls, 2 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Los Angeles IVF Laboratory" is on file.

What these totals cover: FDA records filed under the name "Los Angeles IVF Laboratory".

Latest inspection
Dec 14, 2023 · NAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections2Nov 14, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

FDA record by year

Los Angeles IVF Laboratory's FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

Los Angeles IVF Laboratory: FDA inspections per year 2017: 0 inspections020172018: 1 inspections120182019: 0 inspections020192020: 0 inspections020202021: 0 inspections020212022: 0 inspections020222023: 1 inspections120232024: 0 inspections020242025: 0 inspections020252026: 0 inspections02026
YearInspectionsOAIWarning lettersRecall recordsClass I
202600000
202500000
202400000
202310000
202200000
202100000
202000000
201900000
201810000
201700000

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.

Recent FDA inspections

2 inspections from Oct 19, 2018 to Dec 14, 2023.

DateSiteProductClassificationFEI
Dec 14, 2023Encino, CABiologicsNo Action Indicated (NAI)3014669728
Oct 19, 2018Encino, CABiologicsVoluntary Action Indicated (VAI)3014669728
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.

FacilityLocationInspectionsLatest
FEI 3014669728Encino, CA2Dec 14, 2023

Los Angeles IVF Laboratory and the FDA: common questions

Has Los Angeles IVF Laboratory received an FDA warning letter?

No FDA warning letter addressed to the name "Los Angeles IVF Laboratory" 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 Los Angeles IVF Laboratory received an FDA Form 483?

FDA has not published a Form 483 for "Los Angeles IVF Laboratory" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect Los Angeles IVF Laboratory?

The most recent FDA inspection on file ended Dec 14, 2023 at Encino, CA and was classified NAI. FDA has 2 inspections of Los Angeles IVF Laboratory on file.

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