FDA Inspection 1318024 — Ray Mcdermott

Ray Mcdermott — FEI 3042870708

The FDA completed an inspection of Ray Mcdermott on Apr 17, 2026 in Dublin. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Apr 17, 2026
Fiscal Year
2026
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Dublin (Ireland)

Additional details

Clinical Investigator (CI)

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