FDA Inspection 1182280 — Terumo Medical Corporation

Terumo Medical Corporation — FEI 1118880

The FDA completed an inspection of Terumo Medical Corporation on October 28, 2022 in Elkton, MD. 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
October 28, 2022
Fiscal Year
2023
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Elkton, MD (United States)