FDA Inspection 1278970 — Shandong Lianfa Medical Plastic Products Co., Ltd
The FDA completed an inspection of Shandong Lianfa Medical Plastic Products Co., Ltd on July 24, 2025 in Jinan. 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) (VAI)
- End Date
- July 24, 2025
- Fiscal Year
- 2025
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Jinan (China)