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FDA Inspection
•CSL Behring L.L.C.•May 23, 2019

CSL Behring L.L.C. – FDA Inspection, May 23, 2019

Record Details

This FDA Inspection record concerns CSL Behring L.L.C., with an inspection on May 23, 2019, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
CSL Behring L.L.C.
Inspection Date
May 23, 2019
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
People
  • Mihaly S. Ligmond (FDA Associated Person)
  • Randall L. Morris (FDA Associated Person)
  • Richard T. Riggie (Company Rep)
View Company Profile

ID · e08a34df-b1ea-4be0-8656-604507a418bc

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
1090775
FDA center
Biologics
Project area
Blood and Blood Products
Outcome
Form 483 issued

Other FDA inspections of CSL Behring L.L.C.

13
DateClassificationOfficeProject area
June 25, 2026Not classifiedChicago District Office
March 2, 2023VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
September 24, 2021VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
October 18, 2018VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
July 19, 2017VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
View all 13 other inspections on the company page
Other documents for CSL Behring L.L.C.
  • FDA Inspection 1284730 - 2026-06-25
  • FDA Inspection 1202268 - 2023-03-02
  • FDA Inspection 1153026 - 2021-09-24
  • FDA Inspection 1072948 - 2018-10-18
  • FDA Inspection 1019044 - 2017-07-19

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