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Reproductive Care Center

FDA Regulatory Profile

Reproductive Care Center has 0 FDA recalls, 5 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
May 14, 2025 · VAI

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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
Inspections5Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
May 14, 2025Sandy, UTBiologicsVoluntary Action Indicated (VAI)3005188109
Feb 11, 2022Sandy, UTBiologicsVoluntary Action Indicated (VAI)3005188109
Feb 15, 2017Sandy, UTBiologicsNo Action Indicated (NAI)3005188109
Mar 5, 2013Sandy, UTBiologicsVoluntary Action Indicated (VAI)3005188109
May 7, 2010Sandy, UTBiologicsNo Action Indicated (NAI)3005188109

NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means 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

FacilityLocationInspectionsLatest
FEI 3005188109Sandy, UT5May 14, 2025

FDA data resources

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