FDA Inspection 751330 — Kaiser Permanente Center For Reproductive Health

Kaiser Permanente Center For Reproductive Health — FEI 3004740553

The FDA completed an inspection of Kaiser Permanente Center For Reproductive Health on Oct 26, 2011 in Fremont, 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
Oct 26, 2011
Fiscal Year
2012
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Fremont, CA (United States)

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