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FDA Inspection
•Diamond Institute for Infertility and Menopause•August 11, 2009

Diamond Institute for Infertility and Menopause – FDA Inspection, Aug 11, 2009

Record Details

This FDA Inspection record concerns Diamond Institute for Infertility and Menopause, with an inspection on August 11, 2009, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Diamond Institute for Infertility and Menopause
Inspection Date
August 11, 2009
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · cbef4f23-07e4-4f00-a26c-c26f36dd0f85

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
603926
FDA center
Biologics
Project area
Human Cellular, Tissue, and Gene Therapies

FDA Citations

5
  1. 21 CFR 1271.80(b)Specimen collections not timely
  2. 21 CFR 1271.85(a)Infection with communicable disease agents
  3. 21 CFR 1271.47(a)Procedures for all other requirements
  4. 21 CFR 1271.75(e)Abbreviated procedure
  5. 21 CFR 1271.50(a)Responsible person to determine, document

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Diamond Institute for Infertility and Menopause

7
DateClassificationOfficeProject area
February 22, 2023NAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
February 23, 2022NAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
July 6, 2018NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
July 6, 2016VAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
December 6, 2013NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
View all 7 other inspections on the company page
Other documents for Diamond Institute for Infertility and Menopause
  • FDA Inspection 1198058 - 2023-02-22
  • FDA Inspection 1162967 - 2022-02-23
  • FDA Inspection 1059272 - 2018-07-06
  • FDA Inspection 979157 - 2016-07-06
  • FDA Inspection 860557 - 2013-12-06

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