FDA Inspection
Terumo Medical CorporationTerumo Medical Corporation – FDA Inspection, Oct 23, 2015
Record Details
This FDA Inspection record concerns Terumo Medical Corporation, with an inspection on October 23, 2015, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Terumo Medical Corporation
- Inspection Date
- October 23, 2015
- Product Type
- Devices
View Company Profile
ID · 4d393933-8ed0-49ba-903e-7a39b5ada30e
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 950051
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Terumo Medical Corporation
8| Date | Classification | Office | Project area |
|---|---|---|---|
| September 11, 2026 | Not classified | Baltimore District Office | Compliance: Devices |
| May 1, 2026 | Not classified | Baltimore District Office | |
| October 28, 2022 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 20, 2019 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| January 13, 2017 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Terumo Medical Corporation
- FDA Inspection 1332082 - 2026-09-11
- FDA Inspection 1317212 - 2026-05-01
- FDA Inspection 1182280 - 2022-10-28
- FDA Inspection 1094113 - 2019-06-20
- FDA Inspection 1003680 - 2017-01-13
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