FDA Inspection 1102672 — 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 Sep 12, 2019 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
Sep 12, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Fremont, CA (United States)

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