FDA Inspection 941285 — Huntington Reproductive Center Medical Group

Huntington Reproductive Center Medical Group — FEI 3009565053

The FDA completed an inspection of Huntington Reproductive Center Medical Group on Sep 9, 2015 in Newport Beach, 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 9, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Newport Beach, CA (United States)

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