FDA Inspection 992391 — PARAGON MEDICAL DEVICE (CHANGZHOU) CO., LTD.
The FDA completed an inspection of PARAGON MEDICAL DEVICE (CHANGZHOU) CO., LTD. on Oct 27, 2016 in Changzhou. 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
- Oct 27, 2016
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Changzhou (China)