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FDA Inspection
•Dorotea Holding Co, LLC dba Alamo Biologics; dba Precision Allograft Solutions; dba Biorepository, LLC•September 20, 2024

Dorotea Holding Co, LLC dba Alamo Biologics; dba Precision Allograft Solutions; dba Biorepository, LLC – FDA Inspection, Sep 20, 2024

Record Details

This FDA Inspection record concerns Dorotea Holding Co, LLC dba Alamo Biologics; dba Precision Allograft Solutions; dba Biorepository, LLC, with an inspection on September 20, 2024, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Dorotea Holding Co, LLC dba Alamo Biologics; dba Precision Allograft Solutions; dba Biorepository, LLC
Inspection Date
September 20, 2024
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
People
  • Esther A. Ofori (Issuing Officer)
  • Richard T. Riggie (Company Rep)
View Company Profile

ID · c55e701b-4e42-40dd-863f-ecbf38b47453

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1251236
FDA center
Biologics
Project area
Human Cellular, Tissue, and Gene Therapies

Other FDA inspections of Dorotea Holding Co, LLC dba Alamo Biologics; dba Precision Allograft Solutions; dba Biorepository, LLC

11
DateClassificationOfficeProject area
September 20, 2024NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
December 18, 2019NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
March 22, 2017NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
March 22, 2017NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
March 22, 2017NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
View all 11 other inspections on the company page
Other documents for Dorotea Holding Co, LLC dba Alamo Biologics; dba Precision Allograft Solutions; dba Biorepository, LLC
  • FDA Inspection 1230638 - 2024-09-20
  • FDA Inspection 1115859 - 2019-12-18
  • FDA Inspection 1010229 - 2017-03-22
  • FDA Inspection 1010206 - 2017-03-22
  • FDA Inspection 1008843 - 2017-03-22

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