FDA Inspection 1070962 — Gold Coast IVF

Gold Coast IVF — FEI 3010436541

The FDA completed an inspection of Gold Coast IVF on Oct 17, 2018 in Woodbury, NY. 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
Oct 17, 2018
Fiscal Year
2019
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Woodbury, NY (United States)