# Wenzhou K.L.F. Plastics Co., Ltd. – FDA Inspection, Aug 30, 2018

Source: https://www.keypedia.com/records/fda_inspections/wenzhou-klf-plastics-co-ltd/208a37cc-906c-4417-b6ea-1662c3692d9b
Source feed: FDA_Inspections

> FDA inspection 1068311 of Wenzhou K.L.F. Plastics Co., Ltd., August 30, 2018. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1068311
- Company Name: Wenzhou K.L.F. Plastics Co., Ltd.
- Inspection Date: 2018-08-30
- 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 991908 - 2016-06-02

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/quynh-strandberg/9b582ae6-85f9-4163-8ce6-b179c5fd340e)

Company: https://www.keypedia.com/companies/wenzhou-klf-plastics-co-ltd/8c5d4169-1a48-4af6-8bee-7d7d3bae0713

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