FDA Inspection 1322190 — PENTAX MEDICAL (PENANG) SDN BHD
The FDA completed an inspection of PENTAX MEDICAL (PENANG) SDN BHD on May 13, 2026 in Penang. 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
- May 13, 2026
- Fiscal Year
- 2026
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Penang (Malaysia)