FDA Inspection 1201073 — Huntington Reproductive Center Medical Group

Huntington Reproductive Center Medical Group — FEI 3009565053

The FDA completed an inspection of Huntington Reproductive Center Medical Group on March 28, 2023 in Newport Beach, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 2 citations were issued during this inspection. Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
March 28, 2023
Fiscal Year
2023
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Newport Beach, CA (United States)

Citations

IDCFRDescription
1222921 CFR 1271.50(a)Determination based on screening and testing
1224221 CFR 1271.55(c)Name and personal info on accompanying records