FDA Inspection 1115373 — Huntington Reproductive Center Medical Group

Huntington Reproductive Center Medical Group — FEI 3006501029

The FDA completed an inspection of Huntington Reproductive Center Medical Group on Jan 8, 2020 in Fullerton, CA. 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 8, 2020
Fiscal Year
2020
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Fullerton, CA (United States)

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