FDA Inspection 1181901 — Johns Hopkins Fertility Center

Johns Hopkins Fertility Center — FEI 3003610950

The FDA completed an inspection of Johns Hopkins Fertility Center on Oct 24, 2022 in Lutherville, MD. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 2 citations were issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Oct 24, 2022
Fiscal Year
2023
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Lutherville, MD (United States)

Citations

IDCFRDescription
1222921 CFR 1271.50(a)Determination based on screening and testing
1227721 CFR 1271.75(a)(1)Risk factors, clinical evidence