FDA Inspection 1025928 — Richard Van Allan M.D.

Richard Van Allan M.D. — FEI 3013229070

The FDA completed an inspection of Richard Van Allan M.D. on Jul 21, 2017 in West Hollywood, 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
Jul 21, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
West Hollywood, CA (United States)

Additional details

Clinical Investigator (CI)

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