# FDA Inspection 1074262 - Kunshan Jiehong Nonwoven Product Co., Ltd. - November 06, 2018

Source: https://www.keypedia.com/records/fda_inspections/kunshan-jiehong-nonwoven-product-co-ltd/d176d95f-efe7-4c0e-9b29-0eba0d5310cd
Source feed: FDA_Inspections

> FDA Inspection 1074262 for Kunshan Jiehong Nonwoven Product Co., Ltd. on November 06, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1074262
- Company Name: Kunshan Jiehong Nonwoven Product Co., Ltd.
- Inspection Date: 2018-11-06
- 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/kunshan-jiehong-nonwoven-product-co-ltd/380e1972-b977-4ca1-a04d-b847a6c089c1

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