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FDA Inspection
•IVF/ART Laboratories/JHH at Green Spring Station•August 14, 2025

IVF/ART Laboratories/JHH at Green Spring Station – FDA Inspection, Aug 14, 2025

Record Details

This FDA Inspection record concerns IVF/ART Laboratories/JHH at Green Spring Station, with an inspection on August 14, 2025, issued by the Baltimore District Office, covering biologics.

Company
IVF/ART Laboratories/JHH at Green Spring Station
Inspection Date
August 14, 2025
Product Type
Biologics
Office
Baltimore District Office
Person
  • La-tasha M. Gunter (Issuing Officer)
View Company Profile

ID · 72707aa9-5e54-4fb5-9812-b83fc14ea324

Inspection Facts

Inspection number
1278452
FDA center
Biologics
Project area
Blood and Blood Products
Outcome
Form 483 issued, view the record

FDA Citations

2
  1. 21 CFR 1271.55(b)(3)Name and address on summary
  2. 21 CFR 1271.75(a)(1)Risk factors, clinical evidence

Full citation text and observation details available on the Dashboard.

Other FDA inspections of IVF/ART Laboratories/JHH at Green Spring Station

5
DateClassificationOfficeProject area
October 24, 2022VAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
November 7, 2018NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
February 15, 2017NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
May 27, 2015NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
October 21, 2011NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
Other documents for IVF/ART Laboratories/JHH at Green Spring Station
  • FDA Inspection 1181901 - 2022-10-24
  • FDA Inspection 1072137 - 2018-11-07
  • FDA Inspection 1001710 - 2017-02-15
  • FDA Inspection 927545 - 2015-05-27
  • FDA Inspection 752447 - 2011-10-21

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