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Fairfax Cryobank, Inc.

FDA Regulatory Profile

Fairfax Cryobank, Inc. has 0 FDA recalls, 34 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Sep 10, 2025 · NAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 4, 2026 (checked Nov 8, 2026, unchanged)File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections34Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Sep 10, 2025Austin, TXBiologicsNo Action Indicated (NAI)3005033855
Apr 24, 2025Fairfax, VABiologicsNo Action Indicated (NAI)3004731690
Feb 13, 2025Roseville, MNBiologicsNo Action Indicated (NAI)3000243835
Apr 17, 2024Philadelphia, PABiologicsNo Action Indicated (NAI)3005287828
Dec 21, 2023Pasadena, CABiologicsNo Action Indicated (NAI)3005108367
Aug 24, 2023Fairfax, VABiologicsVoluntary Action Indicated (VAI)3004731690
Jul 20, 2022Philadelphia, PABiologicsNo Action Indicated (NAI)3005287828
Sep 9, 2021Austin, TXBiologicsNo Action Indicated (NAI)3005033855
Nov 1, 2019Roseville, MNBiologicsNo Action Indicated (NAI)3000243835
Mar 20, 2019Fairfax, VABiologicsVoluntary Action Indicated (VAI)3004731690
Nov 29, 2018Philadelphia, PABiologicsNo Action Indicated (NAI)3005287828
Sep 17, 2018Pasadena, CABiologicsNo Action Indicated (NAI)3005108367
Apr 5, 2018Austin, TXBiologicsNo Action Indicated (NAI)3005033855
Mar 29, 2018Roseville, MNBiologicsNo Action Indicated (NAI)3000243835
Oct 25, 2017San Francisco, CABiologicsNo Action Indicated (NAI)3003110346
Dec 1, 2016Fairfax, VABiologicsNo Action Indicated (NAI)3004731690
Nov 30, 2016Philadelphia, PABiologicsNo Action Indicated (NAI)3005287828
Apr 5, 2016San Francisco, CABiologicsNo Action Indicated (NAI)3003110346
Mar 18, 2016Roseville, MNBiologicsNo Action Indicated (NAI)3000243835
Jan 14, 2016Pasadena, CABiologicsNo Action Indicated (NAI)3005108367

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.

FDA-Inspected Facilities

FacilityLocationInspectionsLatest
FEI 3005033855Austin, TX6Sep 10, 2025
FEI 3004731690Fairfax, VA5Apr 24, 2025
FEI 3000243835Roseville, MN7Feb 13, 2025
FEI 3005287828Philadelphia, PA7Apr 17, 2024
FEI 3005108367Pasadena, CA5Dec 21, 2023
FEI 3003110346San Francisco, CA4Oct 25, 2017

FDA data resources

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