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FDA Inspection
•Arthomed, LLC.•January 25, 2023

Arthomed, LLC. – FDA Inspection, Jan 25, 2023

Record Details

This FDA Inspection record concerns Arthomed, LLC., with an inspection on January 25, 2023, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Arthomed, LLC.
Inspection Date
January 25, 2023
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
Person
  • Ivan E. Reyes (Issuing Officer)
View Company Profile

ID · a2580771-7d7e-4d89-9aeb-ee0d658ac101

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1195570
FDA center
Biologics
Project area
Human Cellular, Tissue, and Gene Therapies

Other FDA inspections of Arthomed, LLC.

4
DateClassificationOfficeProject area
February 22, 2019NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
April 26, 2016NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
April 1, 2014VAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
June 19, 2009NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
Other documents for Arthomed, LLC.
  • FDA Inspection 1081409 - 2019-02-22
  • FDA Inspection 971857 - 2016-04-26
  • FDA Inspection 872590 - 2014-04-01
  • FDA Inspection 590672 - 2009-06-19

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