FDA Inspection 1054257 — Siyang Holymed Products Co., Ltd.
The FDA completed an inspection of Siyang Holymed Products Co., Ltd. on Apr 25, 2018 in Suqian. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Apr 25, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Suqian (China)