FDA Inspection
Jiangyin PureMED Products Co., Ltd.Jiangyin PureMED Products Co., Ltd. – FDA Inspection, May 23, 2019
Record Details
This FDA Inspection record concerns Jiangyin PureMED Products Co., Ltd., with an inspection on May 23, 2019, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 508ee327-7939-4305-8f2c-b3b1c33d518f
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1093743
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
Other FDA inspections of Jiangyin PureMED Products Co., Ltd.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| March 31, 2016 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 13, 2013 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Jiangyin PureMED Products Co., Ltd.
- FDA Inspection 979706 - 2016-03-31
- FDA Inspection 850101 - 2013-06-13
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