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FDA Inspection
•Idaho Center for Reproductive Medicine•January 24, 2011

Idaho Center for Reproductive Medicine – FDA Inspection, Jan 24, 2011

Record Details

This FDA Inspection record concerns Idaho Center for Reproductive Medicine, with an inspection on January 24, 2011, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Idaho Center for Reproductive Medicine
Inspection Date
January 24, 2011
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · 5e2c8b5b-8fee-4d68-81d9-c193c9154f96

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
708208
FDA center
Biologics
Project area
Human Cellular, Tissue, and Gene Therapies

FDA Citations

1
  1. 21 CFR 1271.80(c)Manufacturer instructions not followed

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Idaho Center for Reproductive Medicine

8
DateClassificationOfficeProject area
August 29, 2025Not classifiedSeattle District Office
July 10, 2019NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
September 14, 2016NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
July 10, 2014NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
September 6, 2012NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
View all 8 other inspections on the company page
Other documents for Idaho Center for Reproductive Medicine
  • FDA Inspection 1280989 - 2025-08-29
  • FDA Inspection 1099755 - 2019-07-10
  • FDA Inspection 986772 - 2016-09-14
  • FDA Inspection 886763 - 2014-07-10
  • FDA Inspection 797690 - 2012-09-06

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