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FDA Inspection
•Offices for Fertility and Reproductive Medicine, P. C.•March 18, 2016

Offices for Fertility and Reproductive Medicine, P. C. – FDA Inspection, Mar 18, 2016

Record Details

This FDA Inspection record concerns Offices for Fertility and Reproductive Medicine, P. C., with an inspection on March 18, 2016, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Offices for Fertility and Reproductive Medicine, P. C.
Inspection Date
March 18, 2016
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · f14c6cf9-e9e5-4a01-9fe2-b3f744ddc751

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
962764
FDA center
Biologics
Project area
Human Cellular, Tissue, and Gene Therapies

FDA Citations

1
  1. 21 CFR 1271.47(a)Testing, screening, donor eligibility procedures

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Offices for Fertility and Reproductive Medicine, P. C.

4
DateClassificationOfficeProject area
January 31, 2018VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
May 12, 2014NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
September 25, 2012VAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
September 28, 2009VAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
Other documents for Offices for Fertility and Reproductive Medicine, P. C.
  • FDA Inspection 1039314 - 2018-01-31
  • FDA Inspection 878286 - 2014-05-12
  • FDA Inspection 800591 - 2012-09-25
  • FDA Inspection 615020 - 2009-09-28

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