FDA Inspection 1180197 — Steripack Asia Sdn Bhd

Steripack Asia Sdn Bhd — FEI 3009988302

The FDA completed an inspection of Steripack Asia Sdn Bhd on Sep 1, 2022 in Klang. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 1, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
Klang (Malaysia)