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FDA Inspection
•Metropolitan Reproductive Medicine, P.C.•December 14, 2012

Metropolitan Reproductive Medicine, P.C. – FDA Inspection, Dec 14, 2012

Record Details

This FDA Inspection record concerns Metropolitan Reproductive Medicine, P.C., with an inspection on December 14, 2012, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Metropolitan Reproductive Medicine, P.C.
Inspection Date
December 14, 2012
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · 7cd48794-6eb7-4a35-a79d-e682712dfbff

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
810165
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 Metropolitan Reproductive Medicine, P.C.

4
DateClassificationOfficeProject area
October 13, 2022NAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
June 25, 2019NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
January 27, 2017NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
November 25, 2014VAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
Other documents for Metropolitan Reproductive Medicine, P.C.
  • FDA Inspection 1181504 - 2022-10-13
  • FDA Inspection 1094874 - 2019-06-25
  • FDA Inspection 1000715 - 2017-01-27
  • FDA Inspection 904067 - 2014-11-25

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