FDA Inspection 814535 — Huntington Reproductive Center Medical Group

Huntington Reproductive Center Medical Group — FEI 3003253380

The FDA completed an inspection of Huntington Reproductive Center Medical Group on Jan 10, 2013 in Pasadena, 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 10, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Pasadena, CA (United States)

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