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FDA Inspection
•The Abraham J. And Phyllis Katz Cord Blood•March 22, 2018

The Abraham J. And Phyllis Katz Cord Blood – FDA Inspection, Mar 22, 2018

Record Details

This FDA Inspection record concerns The Abraham J. And Phyllis Katz Cord Blood, with an inspection on March 22, 2018, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
The Abraham J. And Phyllis Katz Cord Blood
Inspection Date
March 22, 2018
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
People
  • Gene D. Arcy
  • Nancy L. Neiger (Issuing Officer)
  • Prajakta A. Varadkar (Issuing Officer)
  • Simone E. Pitts (FDA Associated Person)
View Company Profile

ID · 3454af1f-30a5-401d-bee0-3e8e7581e951

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1051259
FDA center
Biologics
Project area
Human Cellular, Tissue, and Gene Therapies
Outcome
Form 483 issued

Other FDA inspections of The Abraham J. And Phyllis Katz Cord Blood

3
DateClassificationOfficeProject area
September 11, 2026NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
September 15, 2023VAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
January 17, 2020VAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
Other documents for The Abraham J. And Phyllis Katz Cord Blood
  • FDA Inspection 1336058 - 2026-09-11
  • FDA Inspection 1217939 - 2023-09-15
  • FDA Inspection 1115313 - 2020-01-17

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