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FDA Inspection
•MCGH/PPG Reproductive Laboratory, LLC•August 8, 2019

MCGH/PPG Reproductive Laboratory, LLC – FDA Inspection, Aug 8, 2019

Record Details

This FDA Inspection record concerns MCGH/PPG Reproductive Laboratory, LLC, with an inspection on August 8, 2019, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
MCGH/PPG Reproductive Laboratory, LLC
Inspection Date
August 8, 2019
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
Person
  • Nicholas M Smith (Issuing Officer)
View Company Profile

ID · cdb50a0f-2635-48ae-b39b-ebacf39d87fe

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1100462
FDA center
Biologics
Project area
Human Cellular, Tissue, and Gene Therapies

Other FDA inspections of MCGH/PPG Reproductive Laboratory, LLC

6
DateClassificationOfficeProject area
July 31, 2026Not classifiedAtlanta District OfficeHuman Cellular, Tissue, and Gene Therapies
April 11, 2023NAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
December 20, 2016NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
December 17, 2014NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
November 14, 2012NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
View all 6 other inspections on the company page
Other documents for MCGH/PPG Reproductive Laboratory, LLC
  • FDA Inspection 1329606 - 2026-07-31
  • FDA Inspection 1204015 - 2023-04-11
  • FDA Inspection 996118 - 2016-12-20
  • FDA Inspection 907542 - 2014-12-17
  • FDA Inspection 807021 - 2012-11-14

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