FDA Inspection 1051855 — Meridian Clinical Research

Meridian Clinical Research — FEI 3013897754

The FDA completed an inspection of Meridian Clinical Research on May 2, 2018 in Savannah, GA. 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
May 2, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Savannah, GA (United States)

Additional Details

Clinical BA/BE