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Talecris Plasma Resources Inc

FDA Regulatory Profile

Talecris Plasma Resources Inc has 0 FDA recalls, 43 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jul 31, 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
Inspections43Nov 10, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jul 31, 2025Monroe, LABiologicsNo Action Indicated (NAI)2377777
Nov 15, 2019Roanoke, VABiologicsNo Action Indicated (NAI)1177724
Sep 6, 2019Pensacola, FLBiologicsNo Action Indicated (NAI)3007213056
Jul 10, 2019Bloomington, ILBiologicsNo Action Indicated (NAI)3005598613
Apr 11, 2019Amarillo, TXBiologicsNo Action Indicated (NAI)3007118687
Aug 22, 2018Champaign, ILBiologicsNo Action Indicated (NAI)3006125704
Jul 25, 2018Oklahoma City, OKBiologicsNo Action Indicated (NAI)3005480118
Jul 13, 2018Roanoke, VABiologicsNo Action Indicated (NAI)1177724
Mar 1, 2018Phenix City, ALBiologicsNo Action Indicated (NAI)1053452
Jan 18, 2018Huntsville, ALBiologicsNo Action Indicated (NAI)3006118895
Dec 1, 2016Monroe, LABiologicsNo Action Indicated (NAI)2377777
Oct 6, 2016Bloomington, ILBiologicsNo Action Indicated (NAI)3005598613
Aug 24, 2016Bloomington, ILBiologicsNo Action Indicated (NAI)3005598613
Aug 23, 2016Champaign, ILBiologicsNo Action Indicated (NAI)3006125704
Aug 11, 2016Amarillo, TXBiologicsNo Action Indicated (NAI)3007118687
Jun 24, 2016Pensacola, FLBiologicsNo Action Indicated (NAI)3007213056
Feb 11, 2016Phenix City, ALBiologicsNo Action Indicated (NAI)1053452
Jul 22, 2015Oklahoma City, OKBiologicsNo Action Indicated (NAI)3005480118
May 20, 2015Roanoke, VABiologicsNo Action Indicated (NAI)1177724
Oct 21, 2014Monroe, LABiologicsNo Action Indicated (NAI)2377777

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 2377777Monroe, LA6Jul 31, 2025
FEI 1177724Roanoke, VA5Nov 15, 2019
FEI 3007213056Pensacola, FL5Sep 6, 2019
FEI 3005598613Bloomington, IL5Jul 10, 2019
FEI 3007118687Amarillo, TX4Apr 11, 2019
FEI 3006125704Champaign, IL4Aug 22, 2018
FEI 3005480118Oklahoma City, OK5Jul 25, 2018
FEI 1053452Phenix City, AL3Mar 1, 2018
FEI 3006118895Huntsville, AL4Jan 18, 2018
FEI 3003887092Fort Worth, TX1Jun 15, 2011
FEI 3005551888Montgomery, AL1Dec 4, 2008

FDA data resources

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