FDA Inspection 1297842 — Family Fertility Center

Family Fertility Center — FEI 3003939664

The FDA completed an inspection of Family Fertility Center on Jan 5, 2026 in Bethlehem, PA. 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
Jan 5, 2026
Fiscal Year
2026
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Bethlehem, PA (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.