FDA Inspection 1001710 — Johns Hopkins Fertility Center

Johns Hopkins Fertility Center — FEI 3003610950

The FDA completed an inspection of Johns Hopkins Fertility Center on Feb 15, 2017 in Lutherville, MD. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Feb 15, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Lutherville, MD (United States)