# FDA Inspection 991908 - Wenzhou K.L.F. Plastics Co., Ltd. - June 02, 2016

Source: https://www.keypedia.com/records/fda_inspections/wenzhou-klf-plastics-co-ltd/8115a2a6-e16e-4acf-8406-fe7d549ff1ee
Source feed: FDA_Inspections

> FDA Inspection 991908 for Wenzhou K.L.F. Plastics Co., Ltd. on June 02, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 991908
- Company Name: Wenzhou K.L.F. Plastics Co., Ltd.
- Inspection Date: 2016-06-02
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1068311 - 2018-08-30](https://www.keypedia.com/records/fda_inspections/wenzhou-klf-plastics-co-ltd/208a37cc-906c-4417-b6ea-1662c3692d9b)

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