FDA Inspection 1229027 — Terumo Cardiovascular Systems Corporation

Terumo Cardiovascular Systems Corporation — FEI 3000204839

The FDA completed an inspection of Terumo Cardiovascular Systems Corporation on Feb 16, 2024 in Elkton, MD. 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
Feb 16, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Elkton, MD (United States)