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FDA Inspection
•WRP Asia Pacific Sdn Bhd•September 27, 2018

WRP Asia Pacific Sdn Bhd – FDA Inspection, Sep 27, 2018

Record Details

This FDA Inspection record concerns WRP Asia Pacific Sdn Bhd, with an inspection on September 27, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company
WRP Asia Pacific Sdn Bhd
Inspection Date
September 27, 2018
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Stephen D. Eich (Company Rep)
View Company Profile

ID · a1def2da-650c-466d-a43f-ed034fd0208d

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1069387
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices
Outcome
Form 483 issued

Other FDA inspections of WRP Asia Pacific Sdn Bhd

1
DateClassificationOfficeProject area
September 13, 2019Not classifiedOffice of Inspections and Investigations
Other documents for WRP Asia Pacific Sdn Bhd
  • FDA Inspection 1136855 - 2019-09-13

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