# FDA Inspection 1093743 - Jiangyin PureMED Products Co., Ltd. - May 23, 2019

Source: https://www.keypedia.com/records/fda_inspections/jiangyin-puremed-products-co-ltd/508ee327-7939-4305-8f2c-b3b1c33d518f
Source feed: FDA_Inspections

> FDA Inspection 1093743 for Jiangyin PureMED Products Co., Ltd. on May 23, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1093743
- Company Name: Jiangyin PureMED Products Co., Ltd.
- Inspection Date: 2019-05-23
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 979706 - 2016-03-31](https://www.keypedia.com/records/fda_inspections/jiangyin-puremed-products-co-ltd/5b81f341-b58a-448e-b41c-e6f8c1665ff7)
- [FDA Inspection 850101 - 2013-06-13](https://www.keypedia.com/records/fda_inspections/jiangyin-puremed-products-co-ltd/38d550e8-be42-48af-aa45-bc3dd72d34f9)

Company: https://www.keypedia.com/companies/jiangyin-puremed-products-co-ltd/9d00b0e8-4ee8-4885-9f9c-645e4ac223f1

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7