FDA Inspection 1043586 — Huntington Reproductive Center Medical Group

Huntington Reproductive Center Medical Group — FEI 3006501046

The FDA completed an inspection of Huntington Reproductive Center Medical Group on Jan 19, 2018 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
Jan 19, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Los Angeles, CA (United States)

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