FDA Inspection 982759 — Cedars-Sinai Medical Center IRB

Cedars-Sinai Medical Center IRB — FEI 2080668

The FDA completed an inspection of Cedars-Sinai Medical Center IRB on April 18, 2016 in Los Angeles, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
April 18, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Los Angeles, CA (United States)

Additional Details

IRB