FDA Inspection 1000840 — Steripack Asia Sdn Bhd
The FDA completed an inspection of Steripack Asia Sdn Bhd on Jan 24, 2017 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
- Jan 24, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Klang (Malaysia)