FDA Inspection 561886 — Terumo Cardiovascular Systems Corporation
The FDA completed an inspection of Terumo Cardiovascular Systems Corporation on Feb 11, 2009 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 11, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Elkton, MD (United States)