FDA Inspection 893699 — Huntington Reproductive Center Medical Group

Huntington Reproductive Center Medical Group — FEI 3006501029

The FDA completed an inspection of Huntington Reproductive Center Medical Group on Sep 3, 2014 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
Sep 3, 2014
Fiscal Year
2014
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Fullerton, CA (United States)

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