# FDA Inspection 850101 - Jiangyin PureMED Products Co., Ltd. - June 13, 2013

Source: https://www.keypedia.com/records/fda_inspections/jiangyin-puremed-products-co-ltd/38d550e8-be42-48af-aa45-bc3dd72d34f9
Source feed: FDA_Inspections

> FDA Inspection 850101 for Jiangyin PureMED Products Co., Ltd. on June 13, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 850101
- Company Name: Jiangyin PureMED Products Co., Ltd.
- Inspection Date: 2013-06-13
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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