FDA Inspection 1093743 — Jiangyin PureMED Products Co., Ltd.
The FDA completed an inspection of Jiangyin PureMED Products Co., Ltd. on May 23, 2019 in Jiangyin. 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
- May 23, 2019
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Jiangyin (China)