FDA Inspection 982064 — Huntington Reproductive Center Medical Group

Huntington Reproductive Center Medical Group — FEI 3006501046

The FDA completed an inspection of Huntington Reproductive Center Medical Group on Feb 2, 2016 in Los Angeles, 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
Feb 2, 2016
Fiscal Year
2016
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Los Angeles, CA (United States)

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