FDA Inspection 1150444 — Scripps IRB

Scripps IRB — FEI 2082658

The FDA completed an inspection of Scripps IRB on Aug 13, 2021 in San Diego, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Aug 13, 2021
Fiscal Year
2021
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
San Diego, CA (United States)

Additional Details

IRB

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