FDA Inspection 1039600 — Elaine Downie, BSD

Elaine Downie, BSD — FEI 3014188546

The FDA completed an inspection of Elaine Downie, BSD on Jan 11, 2018 in Edinburgh. 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
Jan 11, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Edinburgh (United Kingdom)

Additional Details

Clinical Investigator (CI)

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