FDA Inspection 1020979 — Riverside Clinical Research

Riverside Clinical Research — FEI 3013600999

The FDA completed an inspection of Riverside Clinical Research on Jul 21, 2017 in Edgewater, FL. 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
Jul 21, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Edgewater, FL (United States)

Additional details

Clinical Investigator (CI)

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