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FDA Inspection
•IVFMD - Advanced Reproductive Laboratory•February 1, 2012

IVFMD - Advanced Reproductive Laboratory – FDA Inspection, Feb 1, 2012

Record Details

This FDA Inspection record concerns IVFMD - Advanced Reproductive Laboratory, with an inspection on February 1, 2012, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
IVFMD - Advanced Reproductive Laboratory
Inspection Date
February 1, 2012
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · f5681437-b394-4837-a4c3-80fce8c3b8d7

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
765576
FDA center
Biologics
Project area
Human Cellular, Tissue, and Gene Therapies

FDA Citations

2
  1. 21 CFR 1271.85(b)(2)SOP for release; reactive for CMV
  2. 21 CFR 1271.47(d)Departures: recording and justifying

Full citation text and observation details available on the Dashboard.

Other FDA inspections of IVFMD - Advanced Reproductive Laboratory

5
DateClassificationOfficeProject area
August 25, 2025NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
February 16, 2022NAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
June 4, 2019VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
June 30, 2015VAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
June 30, 2015NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
Other documents for IVFMD - Advanced Reproductive Laboratory
  • FDA Inspection 1279855 - 2025-08-25
  • FDA Inspection 1163350 - 2022-02-16
  • FDA Inspection 1091933 - 2019-06-04
  • FDA Inspection 937295 - 2015-06-30
  • FDA Inspection 932643 - 2015-06-30

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