# Jiangyin PureMED Products Co., Ltd. – FDA Inspection, 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 of Jiangyin PureMED Products Co., Ltd., May 23, 2019. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 2 other FDA inspections on record for this company.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 979706 - 2016-03-31
- FDA Inspection 850101 - 2013-06-13

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/thai-t-duong/59737092-2f30-43a7-b23b-36fa7f212c4a)

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