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FDA Inspection
•Northwest Fertility Center•April 20, 2016

Northwest Fertility Center – FDA Inspection, Apr 20, 2016

Record Details

This FDA Inspection record concerns Northwest Fertility Center, with an inspection on April 20, 2016, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Northwest Fertility Center
Inspection Date
April 20, 2016
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · d744b09a-d529-46fa-baf0-5c2895ca0927

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
967702
FDA center
Biologics
Project area
Human Cellular, Tissue, and Gene Therapies

Other FDA inspections of Northwest Fertility Center

6
DateClassificationOfficeProject area
May 1, 2025Not classifiedSeattle District Office
March 10, 2022NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
September 23, 2019NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
August 26, 2014NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
November 2, 2011VAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
View all 6 other inspections on the company page
Other documents for Northwest Fertility Center
  • FDA Inspection 1269121 - 2025-05-01
  • FDA Inspection 1164561 - 2022-03-10
  • FDA Inspection 1102763 - 2019-09-23
  • FDA Inspection 892547 - 2014-08-26
  • FDA Inspection 754223 - 2011-11-02

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