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