FDA Inspection 1069387 — WRP Asia Pacific Sdn Bhd

WRP Asia Pacific Sdn Bhd — FEI 3002808507

The FDA completed an inspection of WRP Asia Pacific Sdn Bhd on Sep 27, 2018 in Sepang. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Sep 27, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Sepang (Malaysia)