# Kunshan Jiehong Nonwoven Product Co., Ltd. – FDA Inspection, Jan 23, 2014

Source: https://www.keypedia.com/records/fda_inspections/kunshan-jiehong-nonwoven-product-co-ltd/8e12624e-7580-44ac-8172-e4ee84a53b55
Source feed: FDA_Inspections

> FDA inspection 868178 of Kunshan Jiehong Nonwoven Product Co., Ltd., January 23, 2014. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 868178
- Company Name: Kunshan Jiehong Nonwoven Product Co., Ltd.
- Inspection Date: 2014-01-23
- 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: 6

## Related Documents

- FDA Inspection 1113686 - 2019-11-21
- FDA Inspection 1074262 - 2018-11-06

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