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FDA Inspection
•Boston IVF - CRMI Holding, LLC•January 9, 2018

Boston IVF - CRMI Holding, LLC – FDA Inspection, Jan 9, 2018

Record Details

This FDA Inspection record concerns Boston IVF - CRMI Holding, LLC, with an inspection on January 9, 2018, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Boston IVF - CRMI Holding, LLC
Inspection Date
January 9, 2018
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
Person
  • Alice C. Silva (Issuing Officer)
View Company Profile

ID · a4968e69-699c-4416-abae-d7e5a435fbd6

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1040885
FDA center
Biologics
Project area
Human Cellular, Tissue, and Gene Therapies

Other FDA inspections of Boston IVF - CRMI Holding, LLC

4
DateClassificationOfficeProject area
December 19, 2019NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
November 26, 2013NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
January 19, 2012NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
November 5, 2009NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
Other documents for Boston IVF - CRMI Holding, LLC
  • FDA Inspection 1114964 - 2019-12-19
  • FDA Inspection 857112 - 2013-11-26
  • FDA Inspection 764356 - 2012-01-19
  • FDA Inspection 625453 - 2009-11-05

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