FDA Inspection
Terumo Medical Products (Hangzhou) Co., Ltd.Terumo Medical Products (Hangzhou) Co., Ltd. – FDA Inspection, Dec 16, 2011
Record Details
This FDA Inspection record concerns Terumo Medical Products (Hangzhou) Co., Ltd., with an inspection on December 16, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- December 16, 2011
- Product Type
- Devices
View Company Profile
ID · ce51212d-ccc9-4403-9d30-a95acc5f6338
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 761927
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Terumo Medical Products (Hangzhou) Co., Ltd.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| July 25, 2018 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 22, 2018 | Not classified | Office of Inspections and Investigations | |
| October 29, 2015 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 21, 2013 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Terumo Medical Products (Hangzhou) Co., Ltd.
- FDA Inspection 1062256 - 2018-07-25
- FDA Inspection 1077793 - 2018-03-22
- FDA Inspection 948623 - 2015-10-29
- FDA Inspection 825404 - 2013-03-21
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