FDA Inspection 1150636 — Susannah K. Eyre, M.D.

Susannah K. Eyre, M.D. — FEI 3020142657

The FDA completed an inspection of Susannah K. Eyre, M.D. on August 13, 2021 in Liverpool. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 13, 2021
Fiscal Year
2021
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Liverpool (United Kingdom)

Additional Details

Clinical Investigator (CI)