FDA Inspection 1336622 — Chongqing Peninsula Medical Technology Co., Ltd.
The FDA completed an inspection of Chongqing Peninsula Medical Technology Co., Ltd. on Sep 10, 2026 in Chongqing. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Sep 10, 2026
- Fiscal Year
- 2026
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Chongqing (China)