FDA Inspection 850101 — Jiangyin PureMED Products Co., Ltd.
The FDA completed an inspection of Jiangyin PureMED Products Co., Ltd. on June 13, 2013 in Jiangyin. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- June 13, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Jiangyin (China)