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FDA Inspection
•Wenzhou K.L.F. Plastics Co., Ltd.•August 30, 2018

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

Record Details

This FDA Inspection record concerns Wenzhou K.L.F. Plastics Co., Ltd., with an inspection on August 30, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company
Wenzhou K.L.F. Plastics Co., Ltd.
Inspection Date
August 30, 2018
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Quynh Strandberg (FDA Associated Person)
View Company Profile

ID · 208a37cc-906c-4417-b6ea-1662c3692d9b

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
1068311
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices
Outcome
Form 483 issued

Other FDA inspections of Wenzhou K.L.F. Plastics Co., Ltd.

1
DateClassificationOfficeProject area
June 2, 2016VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Wenzhou K.L.F. Plastics Co., Ltd.
  • FDA Inspection 991908 - 2016-06-02

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