FDA Inspection 847181 — Kaiser Permanente Center For Reproductive Health

Kaiser Permanente Center For Reproductive Health — FEI 3006304159

The FDA completed an inspection of Kaiser Permanente Center For Reproductive Health on Jun 27, 2013 in Sacramento, 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
Jun 27, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Sacramento, CA (United States)

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