FDA Inspection 1302596 — Catalyst Clinical Research

Catalyst Clinical Research — FEI 3041227597

The FDA completed an inspection of Catalyst Clinical Research on January 16, 2026 in Wilmington, NC. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
January 16, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Wilmington, NC (United States)

Additional Details

Sponsor, Contract Research Organization